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rs77604250

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77604250(C;G)
Make rs77604250(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356713
GeneHLA-B
is asnp
is mentioned by
dbSNPrs77604250
ebirs77604250
HLIrs77604250
Exacrs77604250
Varsomers77604250
Maprs77604250
PheGenIrs77604250
hapmaprs77604250
1000 genomesrs77604250
hgdprs77604250
ensemblrs77604250
gopubmedrs77604250
geneviewrs77604250
scholarrs77604250
googlers77604250
pharmgkbrs77604250
gwascentralrs77604250
openSNPrs77604250
23andMers77604250
23andMe allrs77604250
SNP Nexus

SNPshotrs77604250
SNPdbers77604250
MSV3drs77604250
GWAS Ctlgrs77604250
Max Magnitude0
ClinVar
Risk rs77604250(G;G)
Alt rs77604250(G;G)
Reference rs77604250(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324490G>C
CLNSRC
CLNACC