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rs121909581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909581(C;T)
Make rs121909581(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22639291
GeneC1QA
is asnp
is mentioned by
dbSNPrs121909581
ebirs121909581
HLIrs121909581
Exacrs121909581
Varsomers121909581
Maprs121909581
PheGenIrs121909581
hapmaprs121909581
1000 genomesrs121909581
hgdprs121909581
ensemblrs121909581
gopubmedrs121909581
geneviewrs121909581
scholarrs121909581
googlers121909581
pharmgkbrs121909581
gwascentralrs121909581
openSNPrs121909581
23andMers121909581
23andMe allrs121909581
SNP Nexus

SNPshotrs121909581
SNPdbers121909581
MSV3drs121909581
GWAS Ctlgrs121909581
Max Magnitude0
OMIM120550
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909581(T;T)
Alt rs121909581(T;T)
Reference rs121909581(C;C)
Significance Pathogenic
Disease C1q deficiency
Variation info
Gene C1QA
CLNDBN C1q deficiency
Reversed 0
HGVS NC_000001.10:g.22965784C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018602.27,