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rs2287845

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2287845(C;T)
Make rs2287845(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position6696586
GeneC3
is asnp
is mentioned by
dbSNPrs2287845
dbSNP (classic)rs2287845
ClinGenrs2287845
ebirs2287845
HLIrs2287845
Exacrs2287845
Gnomadrs2287845
Varsomers2287845
LitVarrs2287845
Maprs2287845
PheGenIrs2287845
Biobankrs2287845
1000 genomesrs2287845
hgdprs2287845
ensemblrs2287845
geneviewrs2287845
scholarrs2287845
googlers2287845
pharmgkbrs2287845
gwascentralrs2287845
openSNPrs2287845
23andMers2287845
23andMe allrs2287845
SNPshotrs2287845
SNPdbers2287845
MSV3drs2287845
GWAS Ctlgrs2287845
Max Magnitude0

[PMID 28611769OA-icon.png] Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.


ClinVar
Risk rs2287845(T;T)
Alt rs2287845(T;T)
Reference Rs2287845(C;C)
Significance Non-pathogenic
Disease C3 deficiency Macular degeneration Atypical hemolytic uremic syndrome
Variation info
Gene C3
CLNDBN C3 deficiency Macular degeneration Atypical hemolytic uremic syndrome
Reversed 1
HGVS NC_000019.9:g.6696597G>A
CLNSRC
CLNACC RCV000281934.1, RCV000317538.1, RCV000374021.1,