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rs151341195

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341195(C;T)
Make rs151341195(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356741
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341195
ebirs151341195
HLIrs151341195
Exacrs151341195
Varsomers151341195
Maprs151341195
PheGenIrs151341195
hapmaprs151341195
1000 genomesrs151341195
hgdprs151341195
ensemblrs151341195
gopubmedrs151341195
geneviewrs151341195
scholarrs151341195
googlers151341195
pharmgkbrs151341195
gwascentralrs151341195
openSNPrs151341195
23andMers151341195
23andMe allrs151341195
SNP Nexus

SNPshotrs151341195
SNPdbers151341195
MSV3drs151341195
GWAS Ctlgrs151341195
Max Magnitude0
ClinVar
Risk rs151341195(T;T)
Alt rs151341195(T;T)
Reference rs151341195(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324518G>A
CLNSRC
CLNACC