{{Rsnum
|rsid=966321
|Chromosome=1
|position=4255144
|Orientation=minus
|GMAF=0.4022
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 22.3 | 58.9 | 18.8
| HCB | 14.6 | 52.6 | 32.8
| JPT | 16.1 | 45.5 | 38.4
| YRI | 0.7 | 13.7 | 85.6
| ASW | 5.3 | 28.1 | 66.7
| CHB | 14.6 | 52.6 | 32.8
| CHD | 10.3 | 38.3 | 51.4
| GIH | 30.0 | 57.0 | 13.0
| LWK | 2.8 | 30.6 | 66.7
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.6 | 24.0 | 75.3
| TSI | 17.6 | 46.1 | 36.3
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs966321
|PubMedID=17903294
|Condition=Factor VII
|Gene=Intergenic
|Risk Allele=
|pValue=8.00E-006
|OR=NA
|95CI=
|OA=1
}}

{{PharmGKB
|RSID=rs966321
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:17903294; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study (Initial Sample Size: 1,000 individuals (Framingham); Replication Sample Size: NR). This variant is associated with Factor VII.
|Drugs=
|Drug Classes=
|Diseases=Hematologic Diseases
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356457
}}

{{PMID Auto
|PMID=19340012
|Title=Genome-wide association study of tanning phenotype in a population of European ancestry.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs966321
|overall_frequency_n=47
|overall_frequency_d=124
|overall_frequency=0.379032
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=37
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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