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

rs61759945

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61759945(C;T)
Make rs61759945(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270244
GeneHLA-C
is asnp
is mentioned by
dbSNPrs61759945
ebirs61759945
HLIrs61759945
Exacrs61759945
Varsomers61759945
Maprs61759945
PheGenIrs61759945
hapmaprs61759945
1000 genomesrs61759945
hgdprs61759945
ensemblrs61759945
gopubmedrs61759945
geneviewrs61759945
scholarrs61759945
googlers61759945
pharmgkbrs61759945
gwascentralrs61759945
openSNPrs61759945
23andMers61759945
23andMe allrs61759945
SNP Nexus

SNPshotrs61759945
SNPdbers61759945
MSV3drs61759945
GWAS Ctlgrs61759945
Max Magnitude0
ClinVar
Risk rs61759945(T;T)
Alt rs61759945(T;T)
Reference rs61759945(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238021G>A
CLNSRC
CLNACC