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rs151341196

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341196(A;A)
Make rs151341196(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356725
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341196
ebirs151341196
HLIrs151341196
Exacrs151341196
Varsomers151341196
Maprs151341196
PheGenIrs151341196
hapmaprs151341196
1000 genomesrs151341196
hgdprs151341196
ensemblrs151341196
gopubmedrs151341196
geneviewrs151341196
scholarrs151341196
googlers151341196
pharmgkbrs151341196
gwascentralrs151341196
openSNPrs151341196
23andMers151341196
23andMe allrs151341196
SNP Nexus

SNPshotrs151341196
SNPdbers151341196
MSV3drs151341196
GWAS Ctlgrs151341196
Max Magnitude0
ClinVar
Risk rs151341196(A;A)
Alt rs151341196(A;A)
Reference rs151341196(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324502C>T
CLNSRC
CLNACC