rs2230205

Orientation

minus

Stabilized

minus

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

Make rs2230205(A;A)

Make rs2230205(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

6709693

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs2230205
dbSNP (classic)	rs2230205
ClinGen	rs2230205
ebi	rs2230205
HLI	rs2230205
Exac	rs2230205
Gnomad	rs2230205
Varsome	rs2230205
LitVar	rs2230205
Map	rs2230205
PheGenI	rs2230205
Biobank	rs2230205
1000 genomes	rs2230205
hgdp	rs2230205
ensembl	rs2230205
geneview	rs2230205
scholar	rs2230205
google	rs2230205
pharmgkb	rs2230205
gwascentral	rs2230205
openSNP	rs2230205
23andMe	rs2230205
SNPshot	rs2230205
SNPdbe	rs2230205
MSV3d	rs2230205
GWAS Ctlg	rs2230205

GMAF

0.2098

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 19899988] Association of c3 gene polymorphisms with neovascular age-related macular degeneration in a chinese population

ClinVar
Risk	rs2230205(A;A)
Alt	rs2230205(A;A)
Reference	Rs2230205(G;G)
Significance	Non-pathogenic
Disease	Atypical hemolytic uremic syndrome Macular degeneration C3 deficiency
Variation	info
Gene	C3
CLNDBN	Atypical hemolytic uremic syndrome Macular degeneration C3 deficiency
Reversed	1
HGVS	NC_000019.9:g.6709704C>T
CLNSRC
CLNACC	RCV000266157.1, RCV000318975.1, RCV000358505.1,

[PMID 29742493] Association Between Polymorphisms of the Complement 3 Gene and Schizophrenia in a Han Chinese Population.