rs794729228

Orientation

minus

Stabilized

minus

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

Make rs794729228(C;T)

Make rs794729228(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

6714208

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs794729228
dbSNP (classic)	rs794729228
ClinGen	rs794729228
ebi	rs794729228
HLI	rs794729228
Exac	rs794729228
Gnomad	rs794729228
Varsome	rs794729228
LitVar	rs794729228
Map	rs794729228
PheGenI	rs794729228
Biobank	rs794729228
1000 genomes	rs794729228
hgdp	rs794729228
ensembl	rs794729228
geneview	rs794729228
scholar	rs794729228
google	rs794729228
pharmgkb	rs794729228
gwascentral	rs794729228
openSNP	rs794729228
23andMe	rs794729228
SNPshot	rs794729228
SNPdbe	rs794729228
MSV3d	rs794729228
GWAS Ctlg	rs794729228

Max Magnitude

0

ClinVar
Risk	rs794729228(T;T)
Alt	rs794729228(T;T)
Reference	Rs794729228(C;C)
Significance	Probable-Pathogenic
Disease	Atypical hemolytic-uremic syndrome 5
Variation	info
Gene	C3
CLNDBN	Atypical hemolytic-uremic syndrome 5
Reversed	1
HGVS	NC_000019.9:g.6714219G>A
CLNSRC
CLNACC	RCV000184049.1,