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rs77592474

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77592474(A;A)
Make rs77592474(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356917
GeneHLA-B
is asnp
is mentioned by
dbSNPrs77592474
ebirs77592474
HLIrs77592474
Exacrs77592474
Varsomers77592474
Maprs77592474
PheGenIrs77592474
hapmaprs77592474
1000 genomesrs77592474
hgdprs77592474
ensemblrs77592474
gopubmedrs77592474
geneviewrs77592474
scholarrs77592474
googlers77592474
pharmgkbrs77592474
gwascentralrs77592474
openSNPrs77592474
23andMers77592474
23andMe allrs77592474
SNP Nexus

SNPshotrs77592474
SNPdbers77592474
MSV3drs77592474
GWAS Ctlgrs77592474
Max Magnitude0
ClinVar
Risk rs77592474(A,T;A,T)
Alt rs77592474(A,T;A,T)
Reference rs77592474(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324694C>A; NC_000006.11:g.31324694C>T
CLNSRC
CLNACC