{{Rsnum
|rsid=6442925
|Chromosome=3
|position=4972191
|Orientation=plus
|GMAF=0.1566
|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 | 71.4 | 26.8 | 1.8
| HCB | 87.6 | 12.4 | 0.0
| JPT | 92.9 | 7.1 | 0.0
| YRI | 55.1 | 38.8 | 6.1
| ASW | 59.6 | 35.1 | 5.3
| CHB | 87.6 | 12.4 | 0.0
| CHD | 90.8 | 9.2 | 0.0
| GIH | 42.4 | 48.5 | 9.1
| LWK | 46.3 | 44.4 | 9.3
| MEX | 0.0 | 0.0 | 0.0
| MKK | 51.6 | 36.8 | 11.6
| TSI | 67.7 | 28.3 | 4.0
| HapMapRevision=28
}}
This SNP is is found in an intergenetic part of chromosome 3. Along with [[rs534654]] and [[rs1534891]], [[rs6442925]], is part of a 3-SNP (multi-locus) interaction that is associated with [[bipolar disorder]].{{PMID|18228528|OA=1
}}

{{PMID Auto GWAS
|PMID=21979947
|Trait=None
|Title=A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
|RiskAllele=
|Pval=0.000002
|OR=1.5600
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}