rs111033290
A SNP in the MYO7A gene on chromosome 11. Its most notable genotype is A;A: Usher syndrome type 1 (predicted)
- Gene
- MYO7A
- Location
- Chr 1177,175,465 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadUsher syndrome type 1 (predicted)
- A;GBadCarrier of an Usher syndrome, type 1 mutation
- G;GGoodcommon in clinvar
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MYO7A SNPs
- 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
- rs368341987A;GProbably a benign variantWorth knowing
- rs948962C;Ccommon in clinvarTypical
- rs139889944G;Gcommon in clinvarTypical
Notes
From SNPedia
Notes
aka c.2187+1G>A
A;A
see text and links via main rs-page
A;G
Unaffected in absence of a second mutation in the MYO7A gene
Source and license
Adapted from rs111033290 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.