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rs137854702

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854702(A;G)
Make rs137854702(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356434
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854702
ebirs137854702
HLIrs137854702
Exacrs137854702
Varsomers137854702
Maprs137854702
PheGenIrs137854702
hapmaprs137854702
1000 genomesrs137854702
hgdprs137854702
ensemblrs137854702
gopubmedrs137854702
geneviewrs137854702
scholarrs137854702
googlers137854702
pharmgkbrs137854702
gwascentralrs137854702
openSNPrs137854702
23andMers137854702
23andMe allrs137854702
SNP Nexus

SNPshotrs137854702
SNPdbers137854702
MSV3drs137854702
GWAS Ctlgrs137854702
Max Magnitude0
ClinVar
Risk rs137854702(C,G,T;C,G,T)
Alt rs137854702(C,G,T;C,G,T)
Reference rs137854702(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324211T>A; NC_000006.11:g.31324211T>C; NC_000006.11:g.31324211T>G
CLNSRC
CLNACC