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rs137854696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854696(C;C)
Make rs137854696(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356688
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854696
ebirs137854696
HLIrs137854696
Exacrs137854696
Varsomers137854696
Maprs137854696
PheGenIrs137854696
hapmaprs137854696
1000 genomesrs137854696
hgdprs137854696
ensemblrs137854696
gopubmedrs137854696
geneviewrs137854696
scholarrs137854696
googlers137854696
pharmgkbrs137854696
gwascentralrs137854696
openSNPrs137854696
23andMers137854696
23andMe allrs137854696
SNP Nexus

SNPshotrs137854696
SNPdbers137854696
MSV3drs137854696
GWAS Ctlgrs137854696
Max Magnitude0
ClinVar
Risk rs137854696(A,C,T;A,C,T)
Alt rs137854696(A,C,T;A,C,T)
Reference rs137854696(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324465C>A; NC_000006.11:g.31324465C>G; NC_000006.11:g.31324465C>T
CLNSRC
CLNACC