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rs4679904

From SNPedia

Orientationplus
Stabilizedplus
Make rs4679904(C;C)
Make rs4679904(C;T)
Make rs4679904(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position160623108
is asnp
is mentioned by
dbSNPrs4679904
ebirs4679904
HLIrs4679904
Exacrs4679904
Varsomers4679904
Maprs4679904
PheGenIrs4679904
hapmaprs4679904
1000 genomesrs4679904
hgdprs4679904
ensemblrs4679904
gopubmedrs4679904
geneviewrs4679904
scholarrs4679904
googlers4679904
pharmgkbrs4679904
gwascentralrs4679904
openSNPrs4679904
23andMers4679904
23andMe allrs4679904
SNP Nexus

SNPshotrs4679904
SNPdbers4679904
MSV3drs4679904
GWAS Ctlgrs4679904
GMAF0.186
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19458352OA-icon.png]
Trait Primary biliary cirrhosis
Title Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants
Risk Allele G
P-val 0.000001
Odds Ratio 1.38 [1.21-1.57]


GET Evidence
rs4679904
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary