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rs137854759

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854759(C;C)
Make rs137854759(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356249
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854759
ebirs137854759
HLIrs137854759
Exacrs137854759
Varsomers137854759
Maprs137854759
PheGenIrs137854759
hapmaprs137854759
1000 genomesrs137854759
hgdprs137854759
ensemblrs137854759
gopubmedrs137854759
geneviewrs137854759
scholarrs137854759
googlers137854759
pharmgkbrs137854759
gwascentralrs137854759
openSNPrs137854759
23andMers137854759
23andMe allrs137854759
SNP Nexus

SNPshotrs137854759
SNPdbers137854759
MSV3drs137854759
GWAS Ctlgrs137854759
Max Magnitude0
ClinVar
Risk rs137854759(A,C;A,C)
Alt rs137854759(A,C;A,C)
Reference rs137854759(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324026C>G; NC_000006.11:g.31324026C>T
CLNSRC
CLNACC