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rs151341147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341147(A;A)
Make rs151341147(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356806
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341147
ebirs151341147
HLIrs151341147
Exacrs151341147
Varsomers151341147
Maprs151341147
PheGenIrs151341147
hapmaprs151341147
1000 genomesrs151341147
hgdprs151341147
ensemblrs151341147
gopubmedrs151341147
geneviewrs151341147
scholarrs151341147
googlers151341147
pharmgkbrs151341147
gwascentralrs151341147
openSNPrs151341147
23andMers151341147
23andMe allrs151341147
SNP Nexus

SNPshotrs151341147
SNPdbers151341147
MSV3drs151341147
GWAS Ctlgrs151341147
Merged fromRs151341148
Max Magnitude0
ClinVar
Risk rs151341147(A,C;A,C)
Alt rs151341147(A,C;A,C)
Reference rs151341147(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324583C>G; NC_000006.11:g.31324583C>T
CLNSRC
CLNACC