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rs151341411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341411(C;T)
Make rs151341411(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354439
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341411
dbSNP (classic)rs151341411
ClinGenrs151341411
ebirs151341411
HLIrs151341411
Exacrs151341411
Gnomadrs151341411
Varsomers151341411
LitVarrs151341411
Maprs151341411
PheGenIrs151341411
Biobankrs151341411
1000 genomesrs151341411
hgdprs151341411
ensemblrs151341411
geneviewrs151341411
scholarrs151341411
googlers151341411
pharmgkbrs151341411
gwascentralrs151341411
openSNPrs151341411
23andMers151341411
SNPshotrs151341411
SNPdbers151341411
MSV3drs151341411
GWAS Ctlgrs151341411
Max Magnitude0
ClinVar
Risk rs151341411(T;T)
Alt rs151341411(T;T)
Reference Rs151341411(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322216G>A
CLNSRC
CLNACC