rs1057519482

Orientation

plus

Stabilized

plus

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

Make rs1057519482(A;A)

Make rs1057519482(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1611710

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs1057519482
dbSNP (classic)	rs1057519482
ClinGen	rs1057519482
ebi	rs1057519482
HLI	rs1057519482
Exac	rs1057519482
Gnomad	rs1057519482
Varsome	rs1057519482
LitVar	rs1057519482
Map	rs1057519482
PheGenI	rs1057519482
Biobank	rs1057519482
1000 genomes	rs1057519482
hgdp	rs1057519482
ensembl	rs1057519482
geneview	rs1057519482
scholar	rs1057519482
google	rs1057519482
pharmgkb	rs1057519482
gwascentral	rs1057519482
openSNP	rs1057519482
23andMe	rs1057519482
SNPshot	rs1057519482
SNPdbe	rs1057519482
MSV3d	rs1057519482
GWAS Ctlg	rs1057519482

Max Magnitude

0

ClinVar
Risk	rs1057519482(A;A)
Alt	rs1057519482(A;A)
Reference	Rs1057519482(C;C)
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.1611945C>A
CLNSRC
CLNACC	RCV000416528.1,