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rs151341108

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341108(A;A)
Make rs151341108(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356878
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341108
ebirs151341108
HLIrs151341108
Exacrs151341108
Varsomers151341108
Maprs151341108
PheGenIrs151341108
hapmaprs151341108
1000 genomesrs151341108
hgdprs151341108
ensemblrs151341108
gopubmedrs151341108
geneviewrs151341108
scholarrs151341108
googlers151341108
pharmgkbrs151341108
gwascentralrs151341108
openSNPrs151341108
23andMers151341108
23andMe allrs151341108
SNP Nexus

SNPshotrs151341108
SNPdbers151341108
MSV3drs151341108
GWAS Ctlgrs151341108
Max Magnitude0
ClinVar
Risk rs151341108(A,T;A,T)
Alt rs151341108(A,T;A,T)
Reference rs151341108(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324655G>A; NC_000006.11:g.31324655G>T
CLNSRC
CLNACC