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rs41561812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41561812(C;T)
Make rs41561812(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271045
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41561812
ebirs41561812
HLIrs41561812
Exacrs41561812
Varsomers41561812
Maprs41561812
PheGenIrs41561812
hapmaprs41561812
1000 genomesrs41561812
hgdprs41561812
ensemblrs41561812
gopubmedrs41561812
geneviewrs41561812
scholarrs41561812
googlers41561812
pharmgkbrs41561812
gwascentralrs41561812
openSNPrs41561812
23andMers41561812
23andMe allrs41561812
SNP Nexus

SNPshotrs41561812
SNPdbers41561812
MSV3drs41561812
GWAS Ctlgrs41561812
GMAF0.02893
Max Magnitude0
ClinVar
Risk rs41561812(T;T)
Alt rs41561812(T;T)
Reference rs41561812(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238822G>A
CLNSRC
CLNACC