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rs137854730

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854730(A;A)
Make rs137854730(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356342
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854730
ebirs137854730
HLIrs137854730
Exacrs137854730
Varsomers137854730
Maprs137854730
PheGenIrs137854730
hapmaprs137854730
1000 genomesrs137854730
hgdprs137854730
ensemblrs137854730
gopubmedrs137854730
geneviewrs137854730
scholarrs137854730
googlers137854730
pharmgkbrs137854730
gwascentralrs137854730
openSNPrs137854730
23andMers137854730
23andMe allrs137854730
SNP Nexus

SNPshotrs137854730
SNPdbers137854730
MSV3drs137854730
GWAS Ctlgrs137854730
Max Magnitude0
ClinVar
Risk rs137854730(A,T;A,T)
Alt rs137854730(A,T;A,T)
Reference rs137854730(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324119G>A; NC_000006.11:g.31324119G>T
CLNSRC
CLNACC