rs760676014

Orientation

plus

Stabilized

plus

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

Make rs760676014(C;G)

Make rs760676014(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

1611936

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs760676014
dbSNP (classic)	rs760676014
ClinGen	rs760676014
ebi	rs760676014
HLI	rs760676014
Exac	rs760676014
Gnomad	rs760676014
Varsome	rs760676014
LitVar	rs760676014
Map	rs760676014
PheGenI	rs760676014
Biobank	rs760676014
1000 genomes	rs760676014
hgdp	rs760676014
ensembl	rs760676014
geneview	rs760676014
scholar	rs760676014
google	rs760676014
pharmgkb	rs760676014
gwascentral	rs760676014
openSNP	rs760676014
23andMe	rs760676014
SNPshot	rs760676014
SNPdbe	rs760676014
MSV3d	rs760676014
GWAS Ctlg	rs760676014

Max Magnitude

0

ClinVar
Risk	rs760676014(G;G) rs760676014(T;T)
Alt	rs760676014(G;G) rs760676014(T;T)
Reference	Rs760676014(C;C)
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.1612171C>G
CLNSRC
CLNACC	RCV000416548.1,