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

rs137854735

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854735(C;C)
Make rs137854735(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356329
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854735
ebirs137854735
HLIrs137854735
Exacrs137854735
Varsomers137854735
Maprs137854735
PheGenIrs137854735
hapmaprs137854735
1000 genomesrs137854735
hgdprs137854735
ensemblrs137854735
gopubmedrs137854735
geneviewrs137854735
scholarrs137854735
googlers137854735
pharmgkbrs137854735
gwascentralrs137854735
openSNPrs137854735
23andMers137854735
23andMe allrs137854735
SNP Nexus

SNPshotrs137854735
SNPdbers137854735
MSV3drs137854735
GWAS Ctlgrs137854735
Max Magnitude0
ClinVar
Risk rs137854735(C,T;C,T)
Alt rs137854735(C,T;C,T)
Reference rs137854735(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324106C>A; NC_000006.11:g.31324106C>G
CLNSRC
CLNACC