rs121964917

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs121964917(C;T)

Make rs121964917(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109749594

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964917
dbSNP (classic)	rs121964917
ClinGen	rs121964917
ebi	rs121964917
HLI	rs121964917
Exac	rs121964917
Gnomad	rs121964917
Varsome	rs121964917
LitVar	rs121964917
Map	rs121964917
PheGenI	rs121964917
Biobank	rs121964917
1000 genomes	rs121964917
hgdp	rs121964917
ensembl	rs121964917
geneview	rs121964917
scholar	rs121964917
google	rs121964917
pharmgkb	rs121964917
gwascentral	rs121964917
openSNP	rs121964917
23andMe	rs121964917
SNPshot	rs121964917
SNPdbe	rs121964917
MSV3d	rs121964917
GWAS Ctlg	rs121964917

Max Magnitude

0

OMIM	217030
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121964917(T;T)
Alt	rs121964917(T;T)
Reference	Rs121964917(C;C)
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.110670750G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012908.2,