rs2287845

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs2287845(C;T)

Make rs2287845(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

6696586

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs2287845
dbSNP (classic)	rs2287845
ClinGen	rs2287845
ebi	rs2287845
HLI	rs2287845
Exac	rs2287845
Gnomad	rs2287845
Varsome	rs2287845
LitVar	rs2287845
Map	rs2287845
PheGenI	rs2287845
Biobank	rs2287845
1000 genomes	rs2287845
hgdp	rs2287845
ensembl	rs2287845
geneview	rs2287845
scholar	rs2287845
google	rs2287845
pharmgkb	rs2287845
gwascentral	rs2287845
openSNP	rs2287845
23andMe	rs2287845
SNPshot	rs2287845
SNPdbe	rs2287845
MSV3d	rs2287845
GWAS Ctlg	rs2287845

Max Magnitude

0

[PMID 28611769] 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,