rs121964913

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs121964913(C;T)

Make rs121964913(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109746231

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964913
dbSNP (classic)	rs121964913
ClinGen	rs121964913
ebi	rs121964913
HLI	rs121964913
Exac	rs121964913
Gnomad	rs121964913
Varsome	rs121964913
LitVar	rs121964913
Map	rs121964913
PheGenI	rs121964913
Biobank	rs121964913
1000 genomes	rs121964913
hgdp	rs121964913
ensembl	rs121964913
geneview	rs121964913
scholar	rs121964913
google	rs121964913
pharmgkb	rs121964913
gwascentral	rs121964913
openSNP	rs121964913
23andMe	rs121964913
SNPshot	rs121964913
SNPdbe	rs121964913
MSV3d	rs121964913
GWAS Ctlg	rs121964913

Max Magnitude

0

OMIM	217030
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121964913(T;T)
Alt	rs121964913(T;T)
Reference	Rs121964913(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.110667387G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012904.2,