rs121964915

Orientation

minus

Stabilized

minus

Make rs121964915(A;A)

Make rs121964915(A;G)

Make rs121964915(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109741008

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs121964915
dbSNP (classic)	rs121964915
ClinGen	rs121964915
ebi	rs121964915
HLI	rs121964915
Exac	rs121964915
Gnomad	rs121964915
Varsome	rs121964915
LitVar	rs121964915
Map	rs121964915
PheGenI	rs121964915
Biobank	rs121964915
1000 genomes	rs121964915
hgdp	rs121964915
ensembl	rs121964915
geneview	rs121964915
scholar	rs121964915
google	rs121964915
pharmgkb	rs121964915
gwascentral	rs121964915
openSNP	rs121964915
23andMe	rs121964915
SNPshot	rs121964915
SNPdbe	rs121964915
MSV3d	rs121964915
GWAS Ctlg	rs121964915

Max Magnitude

0

OMIM	217030
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121964915(A;A)
Alt	rs121964915(A;A)
Reference	rs121964915(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.110662164C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012906.2,