rs372221490
A SNP in the ANO5 gene on chromosome 11. Its most notable genotype is A;G: Carrier of a limb-girdle muscular dystrophy, type 2L mutation
- Gene
- ANO5
- Location
- Chr 1122,236,277 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadCarrier of a limb-girdle muscular dystrophy, type 2L mutation
- 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
Notes
From SNPedia
Notes
aka c.762+1G>A
A;G
Unaffected in absence of a second ANO5 gene mutation; see links via main rs-page.
Source and license
Adapted from rs372221490 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.