rs772044176

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs772044176(C;C)

Make rs772044176(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

109764567

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs772044176
dbSNP (classic)	rs772044176
ClinGen	rs772044176
ebi	rs772044176
HLI	rs772044176
Exac	rs772044176
Gnomad	rs772044176
Varsome	rs772044176
LitVar	rs772044176
Map	rs772044176
PheGenI	rs772044176
Biobank	rs772044176
1000 genomes	rs772044176
hgdp	rs772044176
ensembl	rs772044176
geneview	rs772044176
scholar	rs772044176
google	rs772044176
pharmgkb	rs772044176
gwascentral	rs772044176
openSNP	rs772044176
23andMe	rs772044176
SNPshot	rs772044176
SNPdbe	rs772044176
MSV3d	rs772044176
GWAS Ctlg	rs772044176

Max Magnitude

0

ClinVar
Risk	rs772044176(C;C)
Alt	rs772044176(C;C)
Reference	Rs772044176(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CFI
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.110685723T>C
CLNSRC
CLNACC	RCV000413659.1,