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rs61759952

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61759952(C;G)
Make rs61759952(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355477
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759952
ebirs61759952
HLIrs61759952
Exacrs61759952
Varsomers61759952
Maprs61759952
PheGenIrs61759952
hapmaprs61759952
1000 genomesrs61759952
hgdprs61759952
ensemblrs61759952
gopubmedrs61759952
geneviewrs61759952
scholarrs61759952
googlers61759952
pharmgkbrs61759952
gwascentralrs61759952
openSNPrs61759952
23andMers61759952
23andMe allrs61759952
SNP Nexus

SNPshotrs61759952
SNPdbers61759952
MSV3drs61759952
GWAS Ctlgrs61759952
Max Magnitude0
ClinVar
Risk rs61759952(G,T;G,T)
Alt rs61759952(G,T;G,T)
Reference rs61759952(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323254G>A
CLNSRC
CLNACC