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rs151341311

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341311(A;C)
Make rs151341311(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356243
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341311
ebirs151341311
HLIrs151341311
Exacrs151341311
Varsomers151341311
Maprs151341311
PheGenIrs151341311
hapmaprs151341311
1000 genomesrs151341311
hgdprs151341311
ensemblrs151341311
gopubmedrs151341311
geneviewrs151341311
scholarrs151341311
googlers151341311
pharmgkbrs151341311
gwascentralrs151341311
openSNPrs151341311
23andMers151341311
23andMe allrs151341311
SNP Nexus

SNPshotrs151341311
SNPdbers151341311
MSV3drs151341311
GWAS Ctlgrs151341311
Max Magnitude0
ClinVar
Risk rs151341311(C;C)
Alt rs151341311(C;C)
Reference rs151341311(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324020T>G
CLNSRC
CLNACC