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rs151341349

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341349(A;T)
Make rs151341349(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355500
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341349
ebirs151341349
HLIrs151341349
Exacrs151341349
Varsomers151341349
Maprs151341349
PheGenIrs151341349
hapmaprs151341349
1000 genomesrs151341349
hgdprs151341349
ensemblrs151341349
gopubmedrs151341349
geneviewrs151341349
scholarrs151341349
googlers151341349
pharmgkbrs151341349
gwascentralrs151341349
openSNPrs151341349
23andMers151341349
23andMe allrs151341349
SNP Nexus

SNPshotrs151341349
SNPdbers151341349
MSV3drs151341349
GWAS Ctlgrs151341349
Max Magnitude0
ClinVar
Risk rs151341349(T;T)
Alt rs151341349(T;T)
Reference rs151341349(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323277T>A
CLNSRC
CLNACC