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rs151341088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341088(A;A)
Make rs151341088(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356953
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341088
ebirs151341088
HLIrs151341088
Exacrs151341088
Varsomers151341088
Maprs151341088
PheGenIrs151341088
hapmaprs151341088
1000 genomesrs151341088
hgdprs151341088
ensemblrs151341088
gopubmedrs151341088
geneviewrs151341088
scholarrs151341088
googlers151341088
pharmgkbrs151341088
gwascentralrs151341088
openSNPrs151341088
23andMers151341088
23andMe allrs151341088
SNP Nexus

SNPshotrs151341088
SNPdbers151341088
MSV3drs151341088
GWAS Ctlgrs151341088
Merged fromRs151341089
GMAF0.006887
Max Magnitude0
ClinVar
Risk rs151341088(A,G,T;A,G,T)
Alt rs151341088(A,G,T;A,G,T)
Reference rs151341088(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324730G>C; NC_000006.11:g.31324730G>T
CLNSRC
CLNACC