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rs137854695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854695(A;A)
Make rs137854695(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356689
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854695
ebirs137854695
HLIrs137854695
Exacrs137854695
Varsomers137854695
Maprs137854695
PheGenIrs137854695
hapmaprs137854695
1000 genomesrs137854695
hgdprs137854695
ensemblrs137854695
gopubmedrs137854695
geneviewrs137854695
scholarrs137854695
googlers137854695
pharmgkbrs137854695
gwascentralrs137854695
openSNPrs137854695
23andMers137854695
23andMe allrs137854695
SNP Nexus

SNPshotrs137854695
SNPdbers137854695
MSV3drs137854695
GWAS Ctlgrs137854695
Max Magnitude0
ClinVar
Risk rs137854695(A,T;A,T)
Alt rs137854695(A,T;A,T)
Reference rs137854695(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324466G>A; NC_000006.11:g.31324466G>T
CLNSRC
CLNACC