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rs151341099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341099(A;A)
Make rs151341099(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356916
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341099
ebirs151341099
HLIrs151341099
Exacrs151341099
Varsomers151341099
Maprs151341099
PheGenIrs151341099
hapmaprs151341099
1000 genomesrs151341099
hgdprs151341099
ensemblrs151341099
gopubmedrs151341099
geneviewrs151341099
scholarrs151341099
googlers151341099
pharmgkbrs151341099
gwascentralrs151341099
openSNPrs151341099
23andMers151341099
23andMe allrs151341099
SNP Nexus

SNPshotrs151341099
SNPdbers151341099
MSV3drs151341099
GWAS Ctlgrs151341099
Max Magnitude0
ClinVar
Risk rs151341099(A;A)
Alt rs151341099(A;A)
Reference rs151341099(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324693G>T
CLNSRC
CLNACC