rs648298
A SNP in the MYH14 gene on chromosome 19. Its most notable genotype is T;T.
- Gene
- MYH14
- Location
- Chr 1950,189,876 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 35%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableNot ratedNo summary available.
- C;TNot ratedNo summary available.
- C;CNot ratedNo summary available.
SNPedia records rs648298 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageT;T 44% C;T 44% C;C 12%
- European ancestry (Utah)T;T 33% C;T 43% C;C 24%
- Han Chinese (Beijing)T;T 47% C;T 53% C;C 0%
- Japanese (Tokyo)T;T 55% C;T 32% C;C 14%
- Yoruba (Nigeria)T;T 43% C;T 48% C;C 10%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
deafness
Source and license
Adapted from rs648298 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.