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rs7969151

From SNPedia

Orientationplus
Stabilizedplus
Make rs7969151(A;A)
Make rs7969151(A;G)
Make rs7969151(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position53765493
is asnp
is mentioned by
dbSNPrs7969151
ebirs7969151
HLIrs7969151
Exacrs7969151
Varsomers7969151
Maprs7969151
PheGenIrs7969151
hapmaprs7969151
1000 genomesrs7969151
hgdprs7969151
ensemblrs7969151
gopubmedrs7969151
geneviewrs7969151
scholarrs7969151
googlers7969151
pharmgkbrs7969151
gwascentralrs7969151
openSNPrs7969151
23andMers7969151
23andMe allrs7969151
SNP Nexus

SNPshotrs7969151
SNPdbers7969151
MSV3drs7969151
GWAS Ctlgrs7969151
GMAF0.1814
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19340012OA-icon.png]
Trait Tanning
Title Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry
Risk Allele A
P-val 0.000002
Odds Ratio


GET Evidence
rs7969151
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary