rs121964918

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs121964918(A;A)

Make rs121964918(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109741090

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964918
dbSNP (classic)	rs121964918
ClinGen	rs121964918
ebi	rs121964918
HLI	rs121964918
Exac	rs121964918
Gnomad	rs121964918
Varsome	rs121964918
LitVar	rs121964918
Map	rs121964918
PheGenI	rs121964918
Biobank	rs121964918
1000 genomes	rs121964918
hgdp	rs121964918
ensembl	rs121964918
geneview	rs121964918
scholar	rs121964918
google	rs121964918
pharmgkb	rs121964918
gwascentral	rs121964918
openSNP	rs121964918
23andMe	rs121964918
SNPshot	rs121964918
SNPdbe	rs121964918
MSV3d	rs121964918
GWAS Ctlg	rs121964918

Max Magnitude

0

OMIM	217030
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121964918(A;A)
Alt	rs121964918(A;A)
Reference	Rs121964918(G;G)
Significance	Other
Disease	Atypical hemolytic-uremic syndrome 3
Variation	info
Gene	CFI
CLNDBN	Atypical hemolytic-uremic syndrome 3
Reversed	1
HGVS	NC_000004.11:g.110662246C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012909.2,