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rs61759948

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61759948(C;G)
Make rs61759948(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356307
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759948
ebirs61759948
HLIrs61759948
Exacrs61759948
Varsomers61759948
Maprs61759948
PheGenIrs61759948
hapmaprs61759948
1000 genomesrs61759948
hgdprs61759948
ensemblrs61759948
gopubmedrs61759948
geneviewrs61759948
scholarrs61759948
googlers61759948
pharmgkbrs61759948
gwascentralrs61759948
openSNPrs61759948
23andMers61759948
23andMe allrs61759948
SNP Nexus

SNPshotrs61759948
SNPdbers61759948
MSV3drs61759948
GWAS Ctlgrs61759948
Max Magnitude0
ClinVar
Risk rs61759948(G,T;G,T)
Alt rs61759948(G,T;G,T)
Reference rs61759948(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324084G>A; NC_000006.11:g.31324084G>C
CLNSRC
CLNACC