rs1057519479

Orientation

plus

Stabilized

plus

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

Make rs1057519479(-;-)

Make rs1057519479(-;CATCCAGGACATCAAG)

Make rs1057519479(CATCCAGGACATCAAG;CATCCAGGACATCAAG)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1611111

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs1057519479
dbSNP (classic)	rs1057519479
ClinGen	rs1057519479
ebi	rs1057519479
HLI	rs1057519479
Exac	rs1057519479
Gnomad	rs1057519479
Varsome	rs1057519479
LitVar	rs1057519479
Map	rs1057519479
PheGenI	rs1057519479
Biobank	rs1057519479
1000 genomes	rs1057519479
hgdp	rs1057519479
ensembl	rs1057519479
geneview	rs1057519479
scholar	rs1057519479
google	rs1057519479
pharmgkb	rs1057519479
gwascentral	rs1057519479
openSNP	rs1057519479
23andMe	rs1057519479
SNPshot	rs1057519479
SNPdbe	rs1057519479
MSV3d	rs1057519479
GWAS Ctlg	rs1057519479

Max Magnitude

0

ClinVar
Risk	rs1057519479(-;-)
Alt	rs1057519479(-;-)
Reference	Rs1057519479(GCATCCAGGACATCAA;GCATCCAGGACATCAA)
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.1611346_1611361del16
CLNSRC
CLNACC	RCV000416521.1,