rs28937591
A SNP in the OTOF gene on chromosome 2. Its most notable genotype is C;C: deafness expected
- Gene
- OTOF
- Location
- Chr 226,461,756 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- C;CMost notableNot rateddeafness expected
SNPedia records rs28937591 on the minus strand: (C;C), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
deafness
C;C
this is the rare genotype, however it's on the minus strand so 23andMe users will see GG in their RAW data. promethease handles it correctly
Source and license
Adapted from rs28937591 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.