rs387906497

A SNP in the BCAP31 gene on chromosome X. Its most notable genotype is -;-: X-linked adrenoleukodystrophy; symptoms and age of onset highly variable

Gene
BCAP31
Location
Chr X153,725,249 (GRCh38)
Highest magnitude
7.7Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. -;-Most notableBadX-linked adrenoleukodystrophy; symptoms and age of onset highly variableVery important · 7.7
  2. -;GCAGCCAGCCCAGGTGACATGCCGGTBadCarrier of of X-linked adrenoleukodystrophy mutation; AMN symptoms possibleVery important · 4.4
  3. GCAGCCAGCCCAGGTGACATGCCGGT;GCAGCCAGCCCAGGTGACATGCCGGTGoodcommon in clinvarTypical · 0.0

On SNPedia: (-;-), (-;GCAGCCAGCCCAGGTGACATGCCGGT), (GCAGCCAGCCCAGGTGACATGCCGGT;GCAGCCAGCCCAGGTGACATGCCGGT). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Notes

From SNPedia

Notes

c.-18_8del26 (p.Met1_Gly66del)

-;-

e

Source and license

Adapted from rs387906497 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.