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

rs137854736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854736(C;G)
Make rs137854736(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356326
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854736
ebirs137854736
HLIrs137854736
Exacrs137854736
Varsomers137854736
Maprs137854736
PheGenIrs137854736
hapmaprs137854736
1000 genomesrs137854736
hgdprs137854736
ensemblrs137854736
gopubmedrs137854736
geneviewrs137854736
scholarrs137854736
googlers137854736
pharmgkbrs137854736
gwascentralrs137854736
openSNPrs137854736
23andMers137854736
23andMe allrs137854736
SNP Nexus

SNPshotrs137854736
SNPdbers137854736
MSV3drs137854736
GWAS Ctlgrs137854736
Max Magnitude0
ClinVar
Risk rs137854736(G,T;G,T)
Alt rs137854736(G,T;G,T)
Reference rs137854736(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324103G>A; NC_000006.11:g.31324103G>C
CLNSRC
CLNACC