rs1057520780

Orientation

plus

Stabilized

plus

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

Make rs1057520780(G;T)

Make rs1057520780(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

28767739

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs1057520780
dbSNP (classic)	rs1057520780
ClinGen	rs1057520780
ebi	rs1057520780
HLI	rs1057520780
Exac	rs1057520780
Gnomad	rs1057520780
Varsome	rs1057520780
LitVar	rs1057520780
Map	rs1057520780
PheGenI	rs1057520780
Biobank	rs1057520780
1000 genomes	rs1057520780
hgdp	rs1057520780
ensembl	rs1057520780
geneview	rs1057520780
scholar	rs1057520780
google	rs1057520780
pharmgkb	rs1057520780
gwascentral	rs1057520780
openSNP	rs1057520780
23andMe	rs1057520780
SNPshot	rs1057520780
SNPdbe	rs1057520780
MSV3d	rs1057520780
GWAS Ctlg	rs1057520780

Max Magnitude

0

ClinVar
Risk	rs1057520780(T;T)
Alt	rs1057520780(T;T)
Reference	Rs1057520780(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29236945G>T
CLNSRC
CLNACC	RCV000429306.1,