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rs151341185

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341185(A;A)
Make rs151341185(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356766
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341185
ebirs151341185
HLIrs151341185
Exacrs151341185
Varsomers151341185
Maprs151341185
PheGenIrs151341185
hapmaprs151341185
1000 genomesrs151341185
hgdprs151341185
ensemblrs151341185
gopubmedrs151341185
geneviewrs151341185
scholarrs151341185
googlers151341185
pharmgkbrs151341185
gwascentralrs151341185
openSNPrs151341185
23andMers151341185
23andMe allrs151341185
SNP Nexus

SNPshotrs151341185
SNPdbers151341185
MSV3drs151341185
GWAS Ctlgrs151341185
Merged fromRs151341186
Max Magnitude0
ClinVar
Risk rs151341185(A,G,T;A,G,T)
Alt rs151341185(A,G,T;A,G,T)
Reference rs151341185(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324543G>A; NC_000006.11:g.31324543G>C; NC_000006.11:g.31324543G>T
CLNSRC
CLNACC