rs1057519480

Orientation

plus

Stabilized

plus

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

Make rs1057519480(-;-)

Make rs1057519480(-;CT)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1611163

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs1057519480
dbSNP (classic)	rs1057519480
ClinGen	rs1057519480
ebi	rs1057519480
HLI	rs1057519480
Exac	rs1057519480
Gnomad	rs1057519480
Varsome	rs1057519480
LitVar	rs1057519480
Map	rs1057519480
PheGenI	rs1057519480
Biobank	rs1057519480
1000 genomes	rs1057519480
hgdp	rs1057519480
ensembl	rs1057519480
geneview	rs1057519480
scholar	rs1057519480
google	rs1057519480
pharmgkb	rs1057519480
gwascentral	rs1057519480
openSNP	rs1057519480
23andMe	rs1057519480
SNPshot	rs1057519480
SNPdbe	rs1057519480
MSV3d	rs1057519480
GWAS Ctlg	rs1057519480

Max Magnitude

0

ClinVar
Risk	rs1057519480(-;-)
Alt	rs1057519480(-;-)
Reference	Rs1057519480(CT;CT)
Significance	Pathogenic
Disease	Axenfeld-Rieger syndrome type 3
Variation	info
Gene	FOXC1
CLNDBN	Axenfeld-Rieger syndrome type 3
Reversed	0
HGVS	NC_000006.11:g.1611398_1611399delCT
CLNSRC
CLNACC	RCV000416550.1,