rs185790394

Orientation

plus

Stabilized

plus

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

Make rs185790394(C;G)

Make rs185790394(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

1610202

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs185790394
dbSNP (classic)	rs185790394
ClinGen	rs185790394
ebi	rs185790394
HLI	rs185790394
Exac	rs185790394
Gnomad	rs185790394
Varsome	rs185790394
LitVar	rs185790394
Map	rs185790394
PheGenI	rs185790394
Biobank	rs185790394
1000 genomes	rs185790394
hgdp	rs185790394
ensembl	rs185790394
geneview	rs185790394
scholar	rs185790394
google	rs185790394
pharmgkb	rs185790394
gwascentral	rs185790394
openSNP	rs185790394
23andMe	rs185790394
SNPshot	rs185790394
SNPdbe	rs185790394
MSV3d	rs185790394
GWAS Ctlg	rs185790394

Max Magnitude

0

ClinVar
Risk	rs185790394(G;G) rs185790394(T;T)
Alt	rs185790394(G;G) rs185790394(T;T)
Reference	Rs185790394(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.1610437C>T
CLNSRC
CLNACC	RCV000162083.1,