rs111033415
A SNP in the MYO7A gene on chromosome 11. Its most notable genotype is A;G: Carrier of an Usher syndrome type 1B mutation
- Gene
- MYO7A
- Location
- Chr 1177,162,118 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon in clinvar
- A;GMost notableBadCarrier of an Usher syndrome type 1B mutation
On SNPedia: (A;A), (A;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
- rs121965085C;TCarrier of an Usher syndrome type Ib mutationImportant
- rs368341987A;GProbably a benign variantWorth knowing
- rs948962C;Ccommon in clinvarTypical
- rs139889944G;Gcommon in clinvarTypical
Notes
From SNPedia
Notes
aka c.1344-2A>G
A;G
Unaffected in absence of a second MYO7A gene mutation
Source and license
Adapted from rs111033415 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.