rs4010613

A SNP in the ABCD1P4 gene on chromosome X. Its most notable genotype is A;A: X-linked adrenoleukodystrophy; symptoms and age of onset highly variable

Gene
ABCD1P4
Location
Chr X153,743,055 (GRCh38)
Highest magnitude
7.7Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important · 7.7
  2. A;CBadCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleVery important · 4.4
  3. C;CGoodcommon in clinvarTypical · 0.0
  4. C;GBadCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleVery important · 4.4
  5. C;TBadCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleVery important · 4.4
  6. G;GBadX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important · 7.7
  7. T;TBadX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important · 7.7

On SNPedia: (A;A), (A;C), (C;C), (C;G), (C;T), (G;G), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

dbSNP says the gene is ABCD1 on chromosome X. nextbio and jlickbot think it's ABCD1P4 on chr 22. the position given is probably not correct for chrom 22 16870930, since that appears to be in the centromere.

Source and license

Adapted from rs4010613 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.