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rs17094273

From SNPedia

Orientationplus
Stabilizedplus
Make rs17094273(A;A)
Make rs17094273(A;G)
Make rs17094273(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position96637470
is asnp
is mentioned by
dbSNPrs17094273
ebirs17094273
HLIrs17094273
Exacrs17094273
Varsomers17094273
Maprs17094273
PheGenIrs17094273
hapmaprs17094273
1000 genomesrs17094273
hgdprs17094273
ensemblrs17094273
gopubmedrs17094273
geneviewrs17094273
scholarrs17094273
googlers17094273
pharmgkbrs17094273
gwascentralrs17094273
openSNPrs17094273
23andMers17094273
23andMe allrs17094273
SNP Nexus

SNPshotrs17094273
SNPdbers17094273
MSV3drs17094273
GWAS Ctlgrs17094273
GMAF0.1483
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 9E-8
Odds Ratio


GET Evidence
rs17094273
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary