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rs3179865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3179865(A;A)
Make rs3179865(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356417
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3179865
ebirs3179865
HLIrs3179865
Exacrs3179865
Varsomers3179865
Maprs3179865
PheGenIrs3179865
hapmaprs3179865
1000 genomesrs3179865
hgdprs3179865
ensemblrs3179865
gopubmedrs3179865
geneviewrs3179865
scholarrs3179865
googlers3179865
pharmgkbrs3179865
gwascentralrs3179865
openSNPrs3179865
23andMers3179865
23andMe allrs3179865
SNP Nexus

SNPshotrs3179865
SNPdbers3179865
MSV3drs3179865
GWAS Ctlgrs3179865
GMAF0.3618
Max Magnitude0
ClinVar
Risk rs3179865(A,T;A,T)
Alt rs3179865(A,T;A,T)
Reference rs3179865(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324194G>A; NC_000006.11:g.31324194G>T
CLNSRC
CLNACC