Have questions? Visit https://www.reddit.com/r/SNPedia

rs61759943

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759943(A;A)
Make rs61759943(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271114
GeneHLA-C
is asnp
is mentioned by
dbSNPrs61759943
ebirs61759943
HLIrs61759943
Exacrs61759943
Varsomers61759943
Maprs61759943
PheGenIrs61759943
hapmaprs61759943
1000 genomesrs61759943
hgdprs61759943
ensemblrs61759943
gopubmedrs61759943
geneviewrs61759943
scholarrs61759943
googlers61759943
pharmgkbrs61759943
gwascentralrs61759943
openSNPrs61759943
23andMers61759943
23andMe allrs61759943
SNP Nexus

SNPshotrs61759943
SNPdbers61759943
MSV3drs61759943
GWAS Ctlgrs61759943
Max Magnitude0
ClinVar
Risk rs61759943(A,T;A,T)
Alt rs61759943(A,T;A,T)
Reference rs61759943(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238891C>A; NC_000006.11:g.31238891C>T
CLNSRC
CLNACC