rs731506
A SNP in the LOC107986861 gene on chromosome 7. Its most notable genotype is A;A: common in clinvar
- Gene
- LOC107986861
- Location
- Chr 7150,974,896 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs731506 on the minus strand: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in one HapMap population.
- Han Chinese (Beijing)A;A 100%
Related
Other LOC107986861 SNPs
- rs121912511G;TRomano-Ward Long QT SyndromeVery important
- rs199472844A;GRomano-Ward Long QT SyndromeVery important
- rs199472855C;TRomano-Ward Long QT SyndromeVery important
- rs199472856C;TRomano-Ward Long QT SyndromeVery important
- rs199473413C;TRomano-Ward Long QT SyndromeVery important
- rs199473420C;GRomano-Ward Long QT SyndromeVery important
- rs199473421A;GRomano-Ward Long QT SyndromeVery important
- rs199473487G;TRomano-Ward Long QT SyndromeVery important
Source and license
Adapted from rs731506 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.