rs104894937

A SNP in the TAZ gene on chromosome X. Its most notable genotype is C;T: carrier of a Barth syndrome allele

Gene
TAZ
Location
Chr X154,413,549 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;TMost notableBadcarrier of a Barth syndrome alleleImportant · 3.0
  2. T;TGoodcommon in clinvarTypical · 0.0

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

Conditions, medicines and genes

Other TAZ SNPs

All TAZ SNPs

Notes

From SNPedia

Notes

Barth syndrome, also known as 3-Methylglutaconic aciduria type 2

C;T

see discussion at rs104894937

Source and license

Adapted from rs104894937 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.