rs79691946

Orientation

plus

Stabilized

plus

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

Make rs79691946(C;T)

Make rs79691946(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

1611334

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs79691946
dbSNP (classic)	rs79691946
ClinGen	rs79691946
ebi	rs79691946
HLI	rs79691946
Exac	rs79691946
Gnomad	rs79691946
Varsome	rs79691946
LitVar	rs79691946
Map	rs79691946
PheGenI	rs79691946
Biobank	rs79691946
1000 genomes	rs79691946
hgdp	rs79691946
ensembl	rs79691946
geneview	rs79691946
scholar	rs79691946
google	rs79691946
pharmgkb	rs79691946
gwascentral	rs79691946
openSNP	rs79691946
23andMe	rs79691946
SNPshot	rs79691946
SNPdbe	rs79691946
MSV3d	rs79691946
GWAS Ctlg	rs79691946

GMAF

0.03535

Max Magnitude

0

ClinVar
Risk	rs79691946(T;T)
Alt	rs79691946(T;T)
Reference	Rs79691946(C;C)
Significance	Pathogenic
Disease	Iridogoniodysgenesis type1 not specified not provided
Variation	info
Gene	FOXC1
CLNDBN	Iridogoniodysgenesis type1 not specified not provided
Reversed	0
HGVS	NC_000006.11:g.1611569C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023070.3, RCV000153259.4, RCV000162086.1,