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rs61759941

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759941(C;C)
Make rs61759941(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271271
GeneHLA-C
is asnp
is mentioned by
dbSNPrs61759941
ebirs61759941
HLIrs61759941
Exacrs61759941
Varsomers61759941
Maprs61759941
PheGenIrs61759941
hapmaprs61759941
1000 genomesrs61759941
hgdprs61759941
ensemblrs61759941
gopubmedrs61759941
geneviewrs61759941
scholarrs61759941
googlers61759941
pharmgkbrs61759941
gwascentralrs61759941
openSNPrs61759941
23andMers61759941
23andMe allrs61759941
SNP Nexus

SNPshotrs61759941
SNPdbers61759941
MSV3drs61759941
GWAS Ctlgrs61759941
Max Magnitude0
ClinVar
Risk rs61759941(C,T;C,T)
Alt rs61759941(C,T;C,T)
Reference rs61759941(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239048C>A; NC_000006.11:g.31239048C>G
CLNSRC
CLNACC