rs121964914

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common genotype

Make rs121964914(A;T)

Make rs121964914(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109741074

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964914
dbSNP (classic)	rs121964914
ClinGen	rs121964914
ebi	rs121964914
HLI	rs121964914
Exac	rs121964914
Gnomad	rs121964914
Varsome	rs121964914
LitVar	rs121964914
Map	rs121964914
PheGenI	rs121964914
Biobank	rs121964914
1000 genomes	rs121964914
hgdp	rs121964914
ensembl	rs121964914
geneview	rs121964914
scholar	rs121964914
google	rs121964914
pharmgkb	rs121964914
gwascentral	rs121964914
openSNP	rs121964914
23andMe	rs121964914
SNPshot	rs121964914
SNPdbe	rs121964914
MSV3d	rs121964914
GWAS Ctlg	rs121964914

Max Magnitude

0

OMIM	217030
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121964914(T;T)
Alt	rs121964914(T;T)
Reference	Rs121964914(A;A)
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.110662230T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012905.2,