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rs151341218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341218(A;G)
Make rs151341218(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356418
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341218
ebirs151341218
HLIrs151341218
Exacrs151341218
Varsomers151341218
Maprs151341218
PheGenIrs151341218
hapmaprs151341218
1000 genomesrs151341218
hgdprs151341218
ensemblrs151341218
gopubmedrs151341218
geneviewrs151341218
scholarrs151341218
googlers151341218
pharmgkbrs151341218
gwascentralrs151341218
openSNPrs151341218
23andMers151341218
23andMe allrs151341218
SNP Nexus

SNPshotrs151341218
SNPdbers151341218
MSV3drs151341218
GWAS Ctlgrs151341218
Merged fromRs151341219, Rs151341220
Max Magnitude0
ClinVar
Risk rs151341218(C,G,T;C,G,T)
Alt rs151341218(C,G,T;C,G,T)
Reference rs151341218(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324195T>A; NC_000006.11:g.31324195T>C; NC_000006.11:g.31324195T>G
CLNSRC
CLNACC