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rs61759942

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61759942(C;T)
Make rs61759942(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271171
GeneHLA-C
is asnp
is mentioned by
dbSNPrs61759942
ebirs61759942
HLIrs61759942
Exacrs61759942
Varsomers61759942
Maprs61759942
PheGenIrs61759942
hapmaprs61759942
1000 genomesrs61759942
hgdprs61759942
ensemblrs61759942
gopubmedrs61759942
geneviewrs61759942
scholarrs61759942
googlers61759942
pharmgkbrs61759942
gwascentralrs61759942
openSNPrs61759942
23andMers61759942
23andMe allrs61759942
SNP Nexus

SNPshotrs61759942
SNPdbers61759942
MSV3drs61759942
GWAS Ctlgrs61759942
Max Magnitude0
ClinVar
Risk rs61759942(T;T)
Alt rs61759942(T;T)
Reference rs61759942(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238948G>A
CLNSRC
CLNACC