rs121909338

Orientation

plus

Stabilized

plus

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

Make rs121909338(C;T)

Make rs121909338(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

1610833

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs121909338
dbSNP (classic)	rs121909338
ClinGen	rs121909338
ebi	rs121909338
HLI	rs121909338
Exac	rs121909338
Gnomad	rs121909338
Varsome	rs121909338
LitVar	rs121909338
Map	rs121909338
PheGenI	rs121909338
Biobank	rs121909338
1000 genomes	rs121909338
hgdp	rs121909338
ensembl	rs121909338
geneview	rs121909338
scholar	rs121909338
google	rs121909338
pharmgkb	rs121909338
gwascentral	rs121909338
openSNP	rs121909338
23andMe	rs121909338
SNPshot	rs121909338
SNPdbe	rs121909338
MSV3d	rs121909338
GWAS Ctlg	rs121909338

Max Magnitude

0

OMIM	601090
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121909338(T;T)
Alt	rs121909338(T;T)
Reference	Rs121909338(C;C)
Significance	Pathogenic
Disease	Axenfeld-Rieger syndrome type 3 not specified
Variation	info
Gene	FOXC1
CLNDBN	Axenfeld-Rieger syndrome type 3 not specified
Reversed	0
HGVS	NC_000006.11:g.1611068C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008980.2, RCV000173256.1,