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rs151341283

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341283(A;C)
Make rs151341283(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356283
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341283
ebirs151341283
HLIrs151341283
Exacrs151341283
Varsomers151341283
Maprs151341283
PheGenIrs151341283
hapmaprs151341283
1000 genomesrs151341283
hgdprs151341283
ensemblrs151341283
gopubmedrs151341283
geneviewrs151341283
scholarrs151341283
googlers151341283
pharmgkbrs151341283
gwascentralrs151341283
openSNPrs151341283
23andMers151341283
23andMe allrs151341283
SNP Nexus

SNPshotrs151341283
SNPdbers151341283
MSV3drs151341283
GWAS Ctlgrs151341283
Merged fromRs151341284
Max Magnitude0
ClinVar
Risk rs151341283(C,G;C,G)
Alt rs151341283(C,G;C,G)
Reference rs151341283(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324060T>C; NC_000006.11:g.31324060T>G
CLNSRC
CLNACC