rs1057520663

Orientation

plus

Stabilized

plus

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

Make rs1057520663(G;T)

Make rs1057520663(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

28767685

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs1057520663
dbSNP (classic)	rs1057520663
ClinGen	rs1057520663
ebi	rs1057520663
HLI	rs1057520663
Exac	rs1057520663
Gnomad	rs1057520663
Varsome	rs1057520663
LitVar	rs1057520663
Map	rs1057520663
PheGenI	rs1057520663
Biobank	rs1057520663
1000 genomes	rs1057520663
hgdp	rs1057520663
ensembl	rs1057520663
geneview	rs1057520663
scholar	rs1057520663
google	rs1057520663
pharmgkb	rs1057520663
gwascentral	rs1057520663
openSNP	rs1057520663
23andMe	rs1057520663
SNPshot	rs1057520663
SNPdbe	rs1057520663
MSV3d	rs1057520663
GWAS Ctlg	rs1057520663

Max Magnitude

0

ClinVar
Risk	rs1057520663(T;T)
Alt	rs1057520663(T;T)
Reference	Rs1057520663(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29236891G>T
CLNSRC
CLNACC	RCV000425305.1,