rs11156606
A SNP in the ABCD1 gene on chromosome X. Its most notable genotype is A;A: common/normal
- Gene
- ABCD1
- Location
- Chr X153,741,041 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
- Minor allele frequency
- 23%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;A 63%
- European ancestry (Utah)A;A 83%
- Han Chinese (Beijing)A;A 79%
- Japanese (Tokyo)A;A 86%
- Yoruba (Nigeria)A;A 23%
- African ancestry (Southwest US)A;A 28%
- Chinese (Denver)A;A 83%
- Gujarati IndianA;A 77%
- Luhya (Kenya)A;A 18%
- Mexican ancestry (Los Angeles)A;A 86%
- Maasai (Kenya)A;A 47%
- TuscanA;A 86%
Related
Other ABCD1 SNPs
- rs74315277G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs74315278-;-X-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs74315280A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs128624213A;AX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs128624214G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs128624215G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs128624216G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
- rs128624217G;GX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important
Source and license
Adapted from rs11156606 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.