rs376405759

Orientation

plus

Stabilized

plus

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

Make rs376405759(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

6

Position

1610691

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs376405759
dbSNP (classic)	rs376405759
ClinGen	rs376405759
ebi	rs376405759
HLI	rs376405759
Exac	rs376405759
Gnomad	rs376405759
Varsome	rs376405759
LitVar	rs376405759
Map	rs376405759
PheGenI	rs376405759
Biobank	rs376405759
1000 genomes	rs376405759
hgdp	rs376405759
ensembl	rs376405759
geneview	rs376405759
scholar	rs376405759
google	rs376405759
pharmgkb	rs376405759
gwascentral	rs376405759
openSNP	rs376405759
23andMe	rs376405759
SNPshot	rs376405759
SNPdbe	rs376405759
MSV3d	rs376405759
GWAS Ctlg	rs376405759

Max Magnitude

0

ClinVar
Risk	rs376405759(G;G) Rs376405759(T;T)
Alt	rs376405759(G;G) Rs376405759(T;T)
Reference	Rs376405759(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.1610926C>G
CLNSRC
CLNACC	RCV000255621.1,