rs886039568

Orientation

plus

Stabilized

plus

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

Make rs886039568(C;T)

Make rs886039568(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

6

Position

1610701

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs886039568
dbSNP (classic)	rs886039568
ClinGen	rs886039568
ebi	rs886039568
HLI	rs886039568
Exac	rs886039568
Gnomad	rs886039568
Varsome	rs886039568
LitVar	rs886039568
Map	rs886039568
PheGenI	rs886039568
Biobank	rs886039568
1000 genomes	rs886039568
hgdp	rs886039568
ensembl	rs886039568
geneview	rs886039568
scholar	rs886039568
google	rs886039568
pharmgkb	rs886039568
gwascentral	rs886039568
openSNP	rs886039568
23andMe	rs886039568
SNPshot	rs886039568
SNPdbe	rs886039568
MSV3d	rs886039568
GWAS Ctlg	rs886039568

Max Magnitude

0

ClinVar
Risk	rs886039568(T;T)
Alt	rs886039568(T;T)
Reference	Rs886039568(C;C)
Significance	Pathogenic
Disease	not provided Axenfeld-Rieger syndrome type 3
Variation	info
Gene	FOXC1
CLNDBN	not provided Axenfeld-Rieger syndrome type 3
Reversed	0
HGVS	NC_000006.11:g.1610936C>T
CLNSRC
CLNACC	RCV000255576.1, RCV000416497.1,