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rs151341201

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341201(A;A)
Make rs151341201(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356704
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341201
ebirs151341201
HLIrs151341201
Exacrs151341201
Varsomers151341201
Maprs151341201
PheGenIrs151341201
hapmaprs151341201
1000 genomesrs151341201
hgdprs151341201
ensemblrs151341201
gopubmedrs151341201
geneviewrs151341201
scholarrs151341201
googlers151341201
pharmgkbrs151341201
gwascentralrs151341201
openSNPrs151341201
23andMers151341201
23andMe allrs151341201
SNP Nexus

SNPshotrs151341201
SNPdbers151341201
MSV3drs151341201
GWAS Ctlgrs151341201
Merged fromRs151341202, Rs151341203
Max Magnitude0
ClinVar
Risk rs151341201(A,G,T;A,G,T)
Alt rs151341201(A,G,T;A,G,T)
Reference rs151341201(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324481G>A; NC_000006.11:g.31324481G>C; NC_000006.11:g.31324481G>T
CLNSRC
CLNACC