rs796052465

Orientation

plus

Stabilized

plus

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

Make rs796052465(C;T)

Make rs796052465(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767946

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs796052465
dbSNP (classic)	rs796052465
ClinGen	rs796052465
ebi	rs796052465
HLI	rs796052465
Exac	rs796052465
Gnomad	rs796052465
Varsome	rs796052465
LitVar	rs796052465
Map	rs796052465
PheGenI	rs796052465
Biobank	rs796052465
1000 genomes	rs796052465
hgdp	rs796052465
ensembl	rs796052465
geneview	rs796052465
scholar	rs796052465
google	rs796052465
pharmgkb	rs796052465
gwascentral	rs796052465
openSNP	rs796052465
23andMe	rs796052465
SNPshot	rs796052465
SNPdbe	rs796052465
MSV3d	rs796052465
GWAS Ctlg	rs796052465

Max Magnitude

0

ClinVar
Risk	rs796052465(T;T)
Alt	rs796052465(T;T)
Reference	Rs796052465(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29237152C>T
CLNSRC
CLNACC	RCV000187459.2,