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

rs137854676

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854676(A;A)
Make rs137854676(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356792
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854676
ebirs137854676
HLIrs137854676
Exacrs137854676
Varsomers137854676
Maprs137854676
PheGenIrs137854676
hapmaprs137854676
1000 genomesrs137854676
hgdprs137854676
ensemblrs137854676
gopubmedrs137854676
geneviewrs137854676
scholarrs137854676
googlers137854676
pharmgkbrs137854676
gwascentralrs137854676
openSNPrs137854676
23andMers137854676
23andMe allrs137854676
SNP Nexus

SNPshotrs137854676
SNPdbers137854676
MSV3drs137854676
GWAS Ctlgrs137854676
Max Magnitude0
ClinVar
Risk rs137854676(A,C;A,C)
Alt rs137854676(A,C;A,C)
Reference rs137854676(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324569C>G; NC_000006.11:g.31324569C>T
CLNSRC
CLNACC