rs758049059

Orientation

plus

Stabilized

plus

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

Make rs758049059(-;AT)

Make rs758049059(AT;AT)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

109746473

Gene

CFI

is a	snp
is	mentioned by
dbSNP	rs758049059
dbSNP (classic)	rs758049059
ClinGen	rs758049059
ebi	rs758049059
HLI	rs758049059
Exac	rs758049059
Gnomad	rs758049059
Varsome	rs758049059
LitVar	rs758049059
Map	rs758049059
PheGenI	rs758049059
Biobank	rs758049059
1000 genomes	rs758049059
hgdp	rs758049059
ensembl	rs758049059
geneview	rs758049059
scholar	rs758049059
google	rs758049059
pharmgkb	rs758049059
gwascentral	rs758049059
openSNP	rs758049059
23andMe	rs758049059
SNPshot	rs758049059
SNPdbe	rs758049059
MSV3d	rs758049059
GWAS Ctlg	rs758049059

Max Magnitude

0

ClinVar
Risk	rs758049059(AT;AT)
Alt	rs758049059(AT;AT)
Reference	Rs758049059(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CFI
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.110667630_110667631dupAT
CLNSRC
CLNACC	RCV000400152.1,