rs886044143

Orientation

plus

Stabilized

plus

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

Chromosome

6

Position

1610735

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs886044143
dbSNP (classic)	rs886044143
ClinGen	rs886044143
ebi	rs886044143
HLI	rs886044143
Exac	rs886044143
Gnomad	rs886044143
Varsome	rs886044143
LitVar	rs886044143
Map	rs886044143
PheGenI	rs886044143
Biobank	rs886044143
1000 genomes	rs886044143
hgdp	rs886044143
ensembl	rs886044143
geneview	rs886044143
scholar	rs886044143
google	rs886044143
pharmgkb	rs886044143
gwascentral	rs886044143
openSNP	rs886044143
23andMe	rs886044143
SNPshot	rs886044143
SNPdbe	rs886044143
MSV3d	rs886044143
GWAS Ctlg	rs886044143

Max Magnitude

0

ClinVar
Risk	rs886044143(A;A)
Alt	rs886044143(A;A)
Reference	Rs886044143(-;-)
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.1610970dupA
CLNSRC
CLNACC	RCV000330894.1,