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rs35366573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35366573(C;T)
Make rs35366573(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position207785101
GeneCD46
is asnp
is mentioned by
dbSNPrs35366573
dbSNP (classic)rs35366573
ClinGenrs35366573
ebirs35366573
HLIrs35366573
Exacrs35366573
Gnomadrs35366573
Varsomers35366573
LitVarrs35366573
Maprs35366573
PheGenIrs35366573
Biobankrs35366573
1000 genomesrs35366573
hgdprs35366573
ensemblrs35366573
geneviewrs35366573
scholarrs35366573
googlers35366573
pharmgkbrs35366573
gwascentralrs35366573
openSNPrs35366573
23andMers35366573
SNPshotrs35366573
SNPdbers35366573
MSV3drs35366573
GWAS Ctlgrs35366573
Max Magnitude0

[PMID 25710174OA-icon.png] Genetic Analysis of Membrane Cofactor Protein (CD46) of the Complement System in Women with and without Preeclamptic Pregnancies


ClinVar
Risk rs35366573(T;T)
Alt rs35366573(T;T)
Reference Rs35366573(C;C)
Significance Probable-non-pathogenic
Disease Atypical hemolytic uremic syndrome
Variation info
Gene CD46
CLNDBN Atypical hemolytic uremic syndrome
Reversed 0
HGVS NC_000001.10:g.207958446C>T
CLNSRC
CLNACC RCV000405695.1,