rs1057519481

Orientation

plus

Stabilized

plus

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

Make rs1057519481(-;-)

Make rs1057519481(-;AGCGTGGACAACATCATGACGTCGC)

Make rs1057519481(AGCGTGGACAACATCATGACGTCGC;AGCGTGGACAACATCATGACGTCGC)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1611370

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs1057519481
dbSNP (classic)	rs1057519481
ClinGen	rs1057519481
ebi	rs1057519481
HLI	rs1057519481
Exac	rs1057519481
Gnomad	rs1057519481
Varsome	rs1057519481
LitVar	rs1057519481
Map	rs1057519481
PheGenI	rs1057519481
Biobank	rs1057519481
1000 genomes	rs1057519481
hgdp	rs1057519481
ensembl	rs1057519481
geneview	rs1057519481
scholar	rs1057519481
google	rs1057519481
pharmgkb	rs1057519481
gwascentral	rs1057519481
openSNP	rs1057519481
23andMe	rs1057519481
SNPshot	rs1057519481
SNPdbe	rs1057519481
MSV3d	rs1057519481
GWAS Ctlg	rs1057519481

Max Magnitude

0

ClinVar
Risk	rs1057519481(-;-)
Alt	rs1057519481(-;-)
Reference	Rs1057519481(CAGCGTGGACAACATCATGACGTCG;CAGCGTGGACAACATCATGACGTCG)
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.1611605_1611629del25
CLNSRC
CLNACC	RCV000416504.1,