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rs3180379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3180379(G;T)
Make rs3180379(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356714
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3180379
ebirs3180379
HLIrs3180379
Exacrs3180379
Varsomers3180379
Maprs3180379
PheGenIrs3180379
hapmaprs3180379
1000 genomesrs3180379
hgdprs3180379
ensemblrs3180379
gopubmedrs3180379
geneviewrs3180379
scholarrs3180379
googlers3180379
pharmgkbrs3180379
gwascentralrs3180379
openSNPrs3180379
23andMers3180379
23andMe allrs3180379
SNP Nexus

SNPshotrs3180379
SNPdbers3180379
MSV3drs3180379
GWAS Ctlgrs3180379
GMAF0.1451
Max Magnitude0
ClinVar
Risk rs3180379(A,T;A,T)
Alt rs3180379(A,T;A,T)
Reference rs3180379(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324491C>A; NC_000006.11:g.31324491C>T
CLNSRC
CLNACC