rs104894107
A SNP in the FXN gene on chromosome 9. Its most notable genotype is T;T: Friedreich's ataxia
- Gene
- FXN
- Location
- Chr 969,064,942 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- G;TBadcarrier of a Friedreich's ataxia allele
- T;TMost notableBadFriedreich's ataxia
On SNPedia: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other FXN SNPs
- rs56214919G;GFriedreich's ataxiaVery important
- rs104894105C;CFriedreich's ataxiaVery important
- rs104894106T;TFriedreich's ataxiaVery important
- rs104894108A;AFriedreich's ataxiaVery important
- rs138034837T;TFriedreich's ataxiaVery important
- rs138446138-;-Friedreich's ataxiaVery important
- rs138471431C;CFriedreich's ataxiaVery important
- rs138491271-;-Friedreich's ataxiaVery important
Notes
From SNPedia
Notes
rs104894107, also known as c.389G>T, p.Gly130Val or G130V, is a mutation in the FXN gene on chromosome 9. The minor allele of this SNP is associated with Friedreich's ataxia when inherited in two copies or as a compound heterozygote. This SNP is referred to as i5003931 by 23andMe.
Source and license
Adapted from rs104894107 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.