rs1057519471

Orientation

plus

Stabilized

plus

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

Make rs1057519471(-;-)

Make rs1057519471(-;GGGGGCGGCT)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1610545

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs1057519471
dbSNP (classic)	rs1057519471
ClinGen	rs1057519471
ebi	rs1057519471
HLI	rs1057519471
Exac	rs1057519471
Gnomad	rs1057519471
Varsome	rs1057519471
LitVar	rs1057519471
Map	rs1057519471
PheGenI	rs1057519471
Biobank	rs1057519471
1000 genomes	rs1057519471
hgdp	rs1057519471
ensembl	rs1057519471
geneview	rs1057519471
scholar	rs1057519471
google	rs1057519471
pharmgkb	rs1057519471
gwascentral	rs1057519471
openSNP	rs1057519471
23andMe	rs1057519471
SNPshot	rs1057519471
SNPdbe	rs1057519471
MSV3d	rs1057519471
GWAS Ctlg	rs1057519471

Max Magnitude

0

ClinVar
Risk	rs1057519471(-;-)
Alt	rs1057519471(-;-)
Reference	Rs1057519471(GGGGGCGGCT;GGGGGCGGCT)
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.1610780_1610789delGGGGGCGGCT
CLNSRC
CLNACC	RCV000416515.1,