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rs137854737

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854737(A;A)
Make rs137854737(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356318
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854737
ebirs137854737
HLIrs137854737
Exacrs137854737
Varsomers137854737
Maprs137854737
PheGenIrs137854737
hapmaprs137854737
1000 genomesrs137854737
hgdprs137854737
ensemblrs137854737
gopubmedrs137854737
geneviewrs137854737
scholarrs137854737
googlers137854737
pharmgkbrs137854737
gwascentralrs137854737
openSNPrs137854737
23andMers137854737
23andMe allrs137854737
SNP Nexus

SNPshotrs137854737
SNPdbers137854737
MSV3drs137854737
GWAS Ctlgrs137854737
Max Magnitude0
ClinVar
Risk rs137854737(A,G,T;A,G,T)
Alt rs137854737(A,G,T;A,G,T)
Reference rs137854737(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324095G>A; NC_000006.11:g.31324095G>C; NC_000006.11:g.31324095G>T
CLNSRC
CLNACC