rs121909586

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs121909586(C;G)

Make rs121909586(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

6697673

Gene

C3

is a	snp
is	mentioned by
dbSNP	rs121909586
dbSNP (classic)	rs121909586
ClinGen	rs121909586
ebi	rs121909586
HLI	rs121909586
Exac	rs121909586
Gnomad	rs121909586
Varsome	rs121909586
LitVar	rs121909586
Map	rs121909586
PheGenI	rs121909586
Biobank	rs121909586
1000 genomes	rs121909586
hgdp	rs121909586
ensembl	rs121909586
geneview	rs121909586
scholar	rs121909586
google	rs121909586
pharmgkb	rs121909586
gwascentral	rs121909586
openSNP	rs121909586
23andMe	rs121909586
SNPshot	rs121909586
SNPdbe	rs121909586
MSV3d	rs121909586
GWAS Ctlg	rs121909586

Max Magnitude

0

OMIM	120700
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121909586(G;G) rs121909586(T;T)
Alt	rs121909586(G;G) rs121909586(T;T)
Reference	Rs121909586(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.6697684G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018592.3,