rs1057519477

Orientation

plus

Stabilized

plus

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

Make rs1057519477(G;T)

Make rs1057519477(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1610932

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs1057519477
dbSNP (classic)	rs1057519477
ClinGen	rs1057519477
ebi	rs1057519477
HLI	rs1057519477
Exac	rs1057519477
Gnomad	rs1057519477
Varsome	rs1057519477
LitVar	rs1057519477
Map	rs1057519477
PheGenI	rs1057519477
Biobank	rs1057519477
1000 genomes	rs1057519477
hgdp	rs1057519477
ensembl	rs1057519477
geneview	rs1057519477
scholar	rs1057519477
google	rs1057519477
pharmgkb	rs1057519477
gwascentral	rs1057519477
openSNP	rs1057519477
23andMe	rs1057519477
SNPshot	rs1057519477
SNPdbe	rs1057519477
MSV3d	rs1057519477
GWAS Ctlg	rs1057519477

Max Magnitude

0

ClinVar
Risk	rs1057519477(T;T)
Alt	rs1057519477(T;T)
Reference	Rs1057519477(G;G)
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.1611167G>T
CLNSRC
CLNACC	RCV000416545.1,