rs368341987
A SNP in the MYO7A gene on chromosome 11. Its most notable genotype is A;G: Probably a benign variant
- Gene
- MYO7A
- Location
- Chr 1177,179,843 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableNot ratedProbably a benign variant
- G;GGoodcommon in clinvar
On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MYO7A SNPs
- rs111033290A;AUsher syndrome type 1 (predicted)Very important
- rs1052030A;TCarrier of a mutation for deafnessImportant
- rs111033415A;GCarrier of an Usher syndrome type 1B mutationImportant
- rs121965085C;TCarrier of an Usher syndrome type Ib mutationImportant
- rs948962C;Ccommon in clinvarTypical
- rs139889944G;Gcommon in clinvarTypical
Notes
From SNPedia
Notes
aka c.2476G>A (p.Ala826Thr or A826T) This rare variant is now considered in ClinVar (by the single submitter) to be benign, however, some prediction software algorithms predict it's deleterious and some submitters in the past have felt it was pathogenic.
A;G
see discussion on main rs-page
Source and license
Adapted from rs368341987 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.