rs104893958

Orientation

plus

Stabilized

plus

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

Make rs104893958(C;G)

Make rs104893958(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

1610823

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs104893958
dbSNP (classic)	rs104893958
ClinGen	rs104893958
ebi	rs104893958
HLI	rs104893958
Exac	rs104893958
Gnomad	rs104893958
Varsome	rs104893958
LitVar	rs104893958
Map	rs104893958
PheGenI	rs104893958
Biobank	rs104893958
1000 genomes	rs104893958
hgdp	rs104893958
ensembl	rs104893958
geneview	rs104893958
scholar	rs104893958
google	rs104893958
pharmgkb	rs104893958
gwascentral	rs104893958
openSNP	rs104893958
23andMe	rs104893958
SNPshot	rs104893958
SNPdbe	rs104893958
MSV3d	rs104893958
GWAS Ctlg	rs104893958

Max Magnitude

0

OMIM	601090
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893958(A;A) rs104893958(G;G) rs104893958(T;T)
Alt	rs104893958(A;A) rs104893958(G;G) rs104893958(T;T)
Reference	Rs104893958(C;C)
Significance	Pathogenic
Disease	Iridogoniodysgenesis type1
Variation	info
Gene	FOXC1
CLNDBN	Iridogoniodysgenesis type1
Reversed	0
HGVS	NC_000006.11:g.1611058C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008969.3,