rs1057521783

Orientation

plus

Stabilized

plus

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

Make rs1057521783(C;T)

Make rs1057521783(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

28768469

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs1057521783
dbSNP (classic)	rs1057521783
ClinGen	rs1057521783
ebi	rs1057521783
HLI	rs1057521783
Exac	rs1057521783
Gnomad	rs1057521783
Varsome	rs1057521783
LitVar	rs1057521783
Map	rs1057521783
PheGenI	rs1057521783
Biobank	rs1057521783
1000 genomes	rs1057521783
hgdp	rs1057521783
ensembl	rs1057521783
geneview	rs1057521783
scholar	rs1057521783
google	rs1057521783
pharmgkb	rs1057521783
gwascentral	rs1057521783
openSNP	rs1057521783
23andMe	rs1057521783
SNPshot	rs1057521783
SNPdbe	rs1057521783
MSV3d	rs1057521783
GWAS Ctlg	rs1057521783

Max Magnitude

0

ClinVar
Risk	rs1057521783(T;T)
Alt	rs1057521783(T;T)
Reference	Rs1057521783(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29237675C>T
CLNSRC
CLNACC	RCV000439955.1,