{{Rsnum
|rsid=332951
|Chromosome=6
|position=92597090
|Orientation=plus
|GMAF=0.03214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 86.2 | 12.3 | 1.5
| HCB | 91.1 | 8.9 | 0.0
| JPT | 80.0 | 20.0 | 0.0
| YRI | 95.7 | 4.3 | 0.0
| ASW | 98.2 | 1.8 | 0.0
| CHB | 91.1 | 8.9 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 79.0 | 19.0 | 2.0
| LWK | 95.2 | 4.8 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 98.0 | 2.0 | 0.0
| TSI | 92.9 | 7.1 | 0.0
| HapMapRevision=28
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}

[[Rs332951]] is an intergenic SNP, located most closely to the genes [[EPHA7]] (642932 bps) and [[MIR4643]] (1075353 bp). Based on the draft [[Neanderthal]] genome ({{PMID|20448178}}) it is thought the T allele of this SNP may be derived from Neanderthal admixture.