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rs61759946

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759946(C;C)
Make rs61759946(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269382
GeneHLA-C
is asnp
is mentioned by
dbSNPrs61759946
ebirs61759946
HLIrs61759946
Exacrs61759946
Varsomers61759946
Maprs61759946
PheGenIrs61759946
hapmaprs61759946
1000 genomesrs61759946
hgdprs61759946
ensemblrs61759946
gopubmedrs61759946
geneviewrs61759946
scholarrs61759946
googlers61759946
pharmgkbrs61759946
gwascentralrs61759946
openSNPrs61759946
23andMers61759946
23andMe allrs61759946
SNP Nexus

SNPshotrs61759946
SNPdbers61759946
MSV3drs61759946
GWAS Ctlgrs61759946
Max Magnitude0
ClinVar
Risk rs61759946(C;C)
Alt rs61759946(C;C)
Reference rs61759946(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237159C>G
CLNSRC
CLNACC