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rs151341191

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341191(-;-)
Make rs151341191(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356763
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341191
ebirs151341191
HLIrs151341191
Exacrs151341191
Varsomers151341191
Maprs151341191
PheGenIrs151341191
hapmaprs151341191
1000 genomesrs151341191
hgdprs151341191
ensemblrs151341191
gopubmedrs151341191
geneviewrs151341191
scholarrs151341191
googlers151341191
pharmgkbrs151341191
gwascentralrs151341191
openSNPrs151341191
23andMers151341191
23andMe allrs151341191
SNP Nexus

SNPshotrs151341191
SNPdbers151341191
MSV3drs151341191
GWAS Ctlgrs151341191
Max Magnitude0
ClinVar
Risk rs151341191(;)
Alt rs151341191(;)
Reference rs151341191(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324540delT
CLNSRC
CLNACC