rs796052481

Orientation

plus

Stabilized

plus

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

Make rs796052481(A;A)

Make rs796052481(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767950

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs796052481
dbSNP (classic)	rs796052481
ClinGen	rs796052481
ebi	rs796052481
HLI	rs796052481
Exac	rs796052481
Gnomad	rs796052481
Varsome	rs796052481
LitVar	rs796052481
Map	rs796052481
PheGenI	rs796052481
Biobank	rs796052481
1000 genomes	rs796052481
hgdp	rs796052481
ensembl	rs796052481
geneview	rs796052481
scholar	rs796052481
google	rs796052481
pharmgkb	rs796052481
gwascentral	rs796052481
openSNP	rs796052481
23andMe	rs796052481
SNPshot	rs796052481
SNPdbe	rs796052481
MSV3d	rs796052481
GWAS Ctlg	rs796052481

Max Magnitude

0

ClinVar
Risk	rs796052481(A;A)
Alt	rs796052481(A;A)
Reference	Rs796052481(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29237156G>A
CLNSRC
CLNACC	RCV000187483.2,