rs104893952

Orientation

plus

Stabilized

plus

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

Make rs104893952(C;T)

Make rs104893952(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

1610512

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs104893952
dbSNP (classic)	rs104893952
ClinGen	rs104893952
ebi	rs104893952
HLI	rs104893952
Exac	rs104893952
Gnomad	rs104893952
Varsome	rs104893952
LitVar	rs104893952
Map	rs104893952
PheGenI	rs104893952
Biobank	rs104893952
1000 genomes	rs104893952
hgdp	rs104893952
ensembl	rs104893952
geneview	rs104893952
scholar	rs104893952
google	rs104893952
pharmgkb	rs104893952
gwascentral	rs104893952
openSNP	rs104893952
23andMe	rs104893952
SNPshot	rs104893952
SNPdbe	rs104893952
MSV3d	rs104893952
GWAS Ctlg	rs104893952

Max Magnitude

0

OMIM	601090
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104893952(T;T)
Alt	rs104893952(T;T)
Reference	Rs104893952(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.1610747C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008973.3,