rs2241394

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs2241394(C;G)

Make rs2241394(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

6685219

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs2241394
dbSNP (classic)	rs2241394
ClinGen	rs2241394
ebi	rs2241394
HLI	rs2241394
Exac	rs2241394
Gnomad	rs2241394
Varsome	rs2241394
LitVar	rs2241394
Map	rs2241394
PheGenI	rs2241394
Biobank	rs2241394
1000 genomes	rs2241394
hgdp	rs2241394
ensembl	rs2241394
geneview	rs2241394
scholar	rs2241394
google	rs2241394
pharmgkb	rs2241394
gwascentral	rs2241394
openSNP	rs2241394
23andMe	rs2241394
SNPshot	rs2241394
SNPdbe	rs2241394
MSV3d	rs2241394
GWAS Ctlg	rs2241394

GMAF

0.09642

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 20157352] Genetic analysis of typical wet-type age-related macular degeneration and polypoidal choroidal vasculopathy in Japanese population

[PMID 22174912] A Common Complement C3 Variant Is Associated with Protection against Wet Age-Related Macular Degeneration in a Japanese Population

[PMID 23233260] Association between polymorphisms of complement pathway genes and age-related macular degeneration in a Chinese population.

ClinVar
Risk	rs2241394(G;G)
Alt	rs2241394(G;G)
Reference	Rs2241394(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	C3
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.6685230G>C
CLNSRC
CLNACC	RCV000190315.1,