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

rs137854683

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854683(A;A)
Make rs137854683(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356731
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854683
ebirs137854683
HLIrs137854683
Exacrs137854683
Varsomers137854683
Maprs137854683
PheGenIrs137854683
hapmaprs137854683
1000 genomesrs137854683
hgdprs137854683
ensemblrs137854683
gopubmedrs137854683
geneviewrs137854683
scholarrs137854683
googlers137854683
pharmgkbrs137854683
gwascentralrs137854683
openSNPrs137854683
23andMers137854683
23andMe allrs137854683
SNP Nexus

SNPshotrs137854683
SNPdbers137854683
MSV3drs137854683
GWAS Ctlgrs137854683
Max Magnitude0
ClinVar
Risk rs137854683(A,C;A,C)
Alt rs137854683(A,C;A,C)
Reference rs137854683(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324508C>G; NC_000006.11:g.31324508C>T
CLNSRC
CLNACC