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rs61759944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61759944(C;C)
Make rs61759944(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270408
GeneHLA-C
is asnp
is mentioned by
dbSNPrs61759944
ebirs61759944
HLIrs61759944
Exacrs61759944
Varsomers61759944
Maprs61759944
PheGenIrs61759944
hapmaprs61759944
1000 genomesrs61759944
hgdprs61759944
ensemblrs61759944
gopubmedrs61759944
geneviewrs61759944
scholarrs61759944
googlers61759944
pharmgkbrs61759944
gwascentralrs61759944
openSNPrs61759944
23andMers61759944
23andMe allrs61759944
SNP Nexus

SNPshotrs61759944
SNPdbers61759944
MSV3drs61759944
GWAS Ctlgrs61759944
Max Magnitude0
ClinVar
Risk rs61759944(C;C)
Alt rs61759944(C;C)
Reference rs61759944(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238185A>G
CLNSRC
CLNACC