rs796052462

Orientation

plus

Stabilized

plus

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

Make rs796052462(A;A)

Make rs796052462(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767840

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs796052462
dbSNP (classic)	rs796052462
ClinGen	rs796052462
ebi	rs796052462
HLI	rs796052462
Exac	rs796052462
Gnomad	rs796052462
Varsome	rs796052462
LitVar	rs796052462
Map	rs796052462
PheGenI	rs796052462
Biobank	rs796052462
1000 genomes	rs796052462
hgdp	rs796052462
ensembl	rs796052462
geneview	rs796052462
scholar	rs796052462
google	rs796052462
pharmgkb	rs796052462
gwascentral	rs796052462
openSNP	rs796052462
23andMe	rs796052462
SNPshot	rs796052462
SNPdbe	rs796052462
MSV3d	rs796052462
GWAS Ctlg	rs796052462

Max Magnitude

0

ClinVar
Risk	rs796052462(A;A) rs796052462(G;G)
Alt	rs796052462(A;A) rs796052462(G;G)
Reference	Rs796052462(C;C)
Significance	Pathogenic
Disease	not provided Inborn genetic diseases
Variation	info
Gene	FOXG1
CLNDBN	not provided Inborn genetic diseases
Reversed	0
HGVS	NC_000014.8:g.29237046C>A; NC_000014.8:g.29237046C>G
CLNSRC
CLNACC	RCV000187456.2, RCV000190704.1, RCV000255136.1,