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rs151341136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341136(C;C)
Make rs151341136(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356812
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341136
ebirs151341136
HLIrs151341136
Exacrs151341136
Varsomers151341136
Maprs151341136
PheGenIrs151341136
hapmaprs151341136
1000 genomesrs151341136
hgdprs151341136
ensemblrs151341136
gopubmedrs151341136
geneviewrs151341136
scholarrs151341136
googlers151341136
pharmgkbrs151341136
gwascentralrs151341136
openSNPrs151341136
23andMers151341136
23andMe allrs151341136
SNP Nexus

SNPshotrs151341136
SNPdbers151341136
MSV3drs151341136
GWAS Ctlgrs151341136
Merged fromRs151341137, Rs151341138
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs151341136(A,C,T;A,C,T)
Alt rs151341136(A,C,T;A,C,T)
Reference rs151341136(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324589C>A; NC_000006.11:g.31324589C>G; NC_000006.11:g.31324589C>T
CLNSRC
CLNACC