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rs151341192

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341192(A;C)
Make rs151341192(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356763
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341192
ebirs151341192
HLIrs151341192
Exacrs151341192
Varsomers151341192
Maprs151341192
PheGenIrs151341192
hapmaprs151341192
1000 genomesrs151341192
hgdprs151341192
ensemblrs151341192
gopubmedrs151341192
geneviewrs151341192
scholarrs151341192
googlers151341192
pharmgkbrs151341192
gwascentralrs151341192
openSNPrs151341192
23andMers151341192
23andMe allrs151341192
SNP Nexus

SNPshotrs151341192
SNPdbers151341192
MSV3drs151341192
GWAS Ctlgrs151341192
Merged fromRs151341193
Max Magnitude0
ClinVar
Risk rs151341192(C,G;C,G)
Alt rs151341192(C,G;C,G)
Reference rs151341192(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324540T>C; NC_000006.11:g.31324540T>G
CLNSRC
CLNACC