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rs137854701

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854701(A;A)
Make rs137854701(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356435
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854701
ebirs137854701
HLIrs137854701
Exacrs137854701
Varsomers137854701
Maprs137854701
PheGenIrs137854701
hapmaprs137854701
1000 genomesrs137854701
hgdprs137854701
ensemblrs137854701
gopubmedrs137854701
geneviewrs137854701
scholarrs137854701
googlers137854701
pharmgkbrs137854701
gwascentralrs137854701
openSNPrs137854701
23andMers137854701
23andMe allrs137854701
SNP Nexus

SNPshotrs137854701
SNPdbers137854701
MSV3drs137854701
GWAS Ctlgrs137854701
Max Magnitude0
ClinVar
Risk rs137854701(A,G,T;A,G,T)
Alt rs137854701(A,G,T;A,G,T)
Reference rs137854701(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324212G>A; NC_000006.11:g.31324212G>C; NC_000006.11:g.31324212G>T
CLNSRC
CLNACC