rs796052463

Orientation

plus

Stabilized

plus

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

Make rs796052463(C;T)

Make rs796052463(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767865

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs796052463
dbSNP (classic)	rs796052463
ClinGen	rs796052463
ebi	rs796052463
HLI	rs796052463
Exac	rs796052463
Gnomad	rs796052463
Varsome	rs796052463
LitVar	rs796052463
Map	rs796052463
PheGenI	rs796052463
Biobank	rs796052463
1000 genomes	rs796052463
hgdp	rs796052463
ensembl	rs796052463
geneview	rs796052463
scholar	rs796052463
google	rs796052463
pharmgkb	rs796052463
gwascentral	rs796052463
openSNP	rs796052463
23andMe	rs796052463
SNPshot	rs796052463
SNPdbe	rs796052463
MSV3d	rs796052463
GWAS Ctlg	rs796052463

Max Magnitude

0

ClinVar
Risk	rs796052463(T;T)
Alt	rs796052463(T;T)
Reference	Rs796052463(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29237071C>T
CLNSRC
CLNACC	RCV000187457.1,