Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341183

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341183(A;C)
Make rs151341183(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356767
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341183
ebirs151341183
HLIrs151341183
Exacrs151341183
Varsomers151341183
Maprs151341183
PheGenIrs151341183
hapmaprs151341183
1000 genomesrs151341183
hgdprs151341183
ensemblrs151341183
gopubmedrs151341183
geneviewrs151341183
scholarrs151341183
googlers151341183
pharmgkbrs151341183
gwascentralrs151341183
openSNPrs151341183
23andMers151341183
23andMe allrs151341183
SNP Nexus

SNPshotrs151341183
SNPdbers151341183
MSV3drs151341183
GWAS Ctlgrs151341183
Max Magnitude0
ClinVar
Risk rs151341183(C,G;C,G)
Alt rs151341183(C,G;C,G)
Reference rs151341183(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324544T>C; NC_000006.11:g.31324544T>G
CLNSRC
CLNACC