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rs966321

From SNPedia

Orientationminus
Stabilizedminus
Make rs966321(A;A)
Make rs966321(A;C)
Make rs966321(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position4255144
is asnp
is mentioned by
dbSNPrs966321
ebirs966321
HLIrs966321
Exacrs966321
Varsomers966321
Maprs966321
PheGenIrs966321
hapmaprs966321
1000 genomesrs966321
hgdprs966321
ensemblrs966321
gopubmedrs966321
geneviewrs966321
scholarrs966321
googlers966321
pharmgkbrs966321
gwascentralrs966321
openSNPrs966321
23andMers966321
23andMe allrs966321
SNP Nexus

SNPshotrs966321
SNPdbers966321
MSV3drs966321
GWAS Ctlgrs966321
GMAF0.4022
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs966321
PubMedID [PMID 17903294OA-icon.png]
Condition Factor VII
Gene Intergenic
Risk Allele
pValue 8.00E-006
OR NA
95% CI



[PMID 19340012OA-icon.png] Genome-wide association study of tanning phenotype in a population of European ancestry.


GET Evidence
rs966321
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.379032
summary