rs121909585

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs121909585(A;A)

Make rs121909585(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

6692971

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs121909585
dbSNP (classic)	rs121909585
ClinGen	rs121909585
ebi	rs121909585
HLI	rs121909585
Exac	rs121909585
Gnomad	rs121909585
Varsome	rs121909585
LitVar	rs121909585
Map	rs121909585
PheGenI	rs121909585
Biobank	rs121909585
1000 genomes	rs121909585
hgdp	rs121909585
ensembl	rs121909585
geneview	rs121909585
scholar	rs121909585
google	rs121909585
pharmgkb	rs121909585
gwascentral	rs121909585
openSNP	rs121909585
23andMe	rs121909585
SNPshot	rs121909585
SNPdbe	rs121909585
MSV3d	rs121909585
GWAS Ctlg	rs121909585

Max Magnitude

0

OMIM	120700
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909585(A;A)
Alt	rs121909585(A;A)
Reference	Rs121909585(G;G)
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.6692982C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018591.3,