ABCD1
86 SNPs in the ABCD1 gene, 84 with a genotype of magnitude 2 or higher.
- Type
- Gene
- SNPs
- 86
- Notable
- 84Magnitude 2 or higher
- Well documented
- 1
- Genosets
- 0
ABCD1 SNPs
Every genotype, as shown in 23andMe and AncestryDNA files.
- rs11156606Typical
- rs4010613Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;Ccommon in clinvarGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs74315277Very important
- rs74315278Very important
- rs74315280Very important
- rs128624213Very important
- rs128624214Very important
- rs128624215Very important
- C;Ccommon in clinvarGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs128624216Very important
- rs128624217Very important
- rs128624218Very important
- rs128624219Very important
- rs128624220Very important
- rs128624221Very important
- rs128624222Very important
- rs128624223Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;Ccommon in clinvarGood
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs128624224Very important
- C;Ccommon in clinvarGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs128624225Very important
- rs141446687Very important
- rs145073701Very important
- rs146525445Very important
- rs150346282Very important
- rs193922093Very important
- rs193922094Very important
- rs193922097Very important
- rs193922098Very important
- rs201114595Very important
- rs201427153Very important
- rs201568579Very important
- rs202125585Very important
- rs373957035Very important
- rs387906494Very important
- rs387906495Very important
- rs387906496Very important
- rs398123100Very important
- rs398123102Very important
- rs398123103Very important
- rs398123104Very important
- rs398123105Very important
- C;Ccommon in clinvarGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs398123106Very important
- rs398123107Very important
- rs398123108Very important
- rs398123109Very important
- rs398123110Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;Gcommon in clinvarGood
- G;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs398123111Very important
- rs398123112Very important
- -;-X-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- -;GGTGGCCCACGCCTACCGCCTCTCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- GGTGGCCCACGCCTACCGCCTCT;GGTGGCCCACGCCTACCGCCTCTcommon in clinvarGood
- TCTGGTGGCCCACGCCTACCGCC;TCTGGTGGCCCACGCCTACCGCCcommon in clinvarGood
- rs398123113Very important
- rs713993050Very important
- rs727503786Very important
- C;Ccommon in clinvarGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs781797609Very important
- rs781862879Very important
- rs781904944Very important
- rs781924420Very important
- rs781948018Very important
- rs781951552Very important
- rs782083931Very important
- rs782158792Very important
- rs782178199Very important
- rs782230740Very important
- rs782311214Very important
- rs782325478Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;Ccommon/normalGood
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs782370364Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;Ccommon/normalGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs782509393Very important
- C;Ccommon/normalGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs782567454Very important
- rs782567718Very important
- rs782635828Very important
- rs782726660Very important
- rs782747420Very important
- rs782760033Very important
- rs797044610Very important
- rs797044611Very important
- rs797044625Very important
- rs797044626Very important
- rs797044726Very important
- rs797044781Very important
- rs868911300Very important
- rs868934170Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;Ccommon/normalGood
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs886044777Very important
- rs886044882Very important
- rs886044887Very important
- rs1057516052Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of X-linked adrenoleukodystrophy mutation; probably unaffectedBad
- C;Ccommon in clinvarGood
- C;TCarrier of X-linked adrenoleukodystrophy mutation; probably unaffectedBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs1057517954Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;CX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- C;GCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- G;Gcommon in clinvarGood
- G;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs1064793877Very important
- rs1131691743Very important
- A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- A;CCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- C;Ccommon/normalGood
- C;TCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleBad
- T;TX-linked adrenoleukodystrophy; symptoms and age of onset highly variableBad
- rs782041940Very important
No matches.
Other SNPs
No notable genotype or detailed notes
Show 1 SNP
Source and license
Adapted from ABCD1 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.