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rs151341205

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341205(C;G)
Make rs151341205(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356700
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341205
ebirs151341205
HLIrs151341205
Exacrs151341205
Varsomers151341205
Maprs151341205
PheGenIrs151341205
hapmaprs151341205
1000 genomesrs151341205
hgdprs151341205
ensemblrs151341205
gopubmedrs151341205
geneviewrs151341205
scholarrs151341205
googlers151341205
pharmgkbrs151341205
gwascentralrs151341205
openSNPrs151341205
23andMers151341205
23andMe allrs151341205
SNP Nexus

SNPshotrs151341205
SNPdbers151341205
MSV3drs151341205
GWAS Ctlgrs151341205
Max Magnitude0
ClinVar
Risk rs151341205(G,T;G,T)
Alt rs151341205(G,T;G,T)
Reference rs151341205(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324477G>A; NC_000006.11:g.31324477G>C
CLNSRC
CLNACC