rs121909584

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs121909584(C;T)

Make rs121909584(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

6693033

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs121909584
dbSNP (classic)	rs121909584
ClinGen	rs121909584
ebi	rs121909584
HLI	rs121909584
Exac	rs121909584
Gnomad	rs121909584
Varsome	rs121909584
LitVar	rs121909584
Map	rs121909584
PheGenI	rs121909584
Biobank	rs121909584
1000 genomes	rs121909584
hgdp	rs121909584
ensembl	rs121909584
geneview	rs121909584
scholar	rs121909584
google	rs121909584
pharmgkb	rs121909584
gwascentral	rs121909584
openSNP	rs121909584
23andMe	rs121909584
SNPshot	rs121909584
SNPdbe	rs121909584
MSV3d	rs121909584
GWAS Ctlg	rs121909584

Max Magnitude

0

OMIM	120700
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909584(T;T)
Alt	rs121909584(T;T)
Reference	Rs121909584(C;C)
Significance	Other
Disease	Atypical hemolytic-uremic syndrome 5
Variation	info
Gene	C3
CLNDBN	Atypical hemolytic-uremic syndrome 5
Reversed	1
HGVS	NC_000019.9:g.6693044G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018590.3,