rs786205001

Orientation

plus

Stabilized

plus

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

Make rs786205001(-;-)

Make rs786205001(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767535

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs786205001
dbSNP (classic)	rs786205001
ClinGen	rs786205001
ebi	rs786205001
HLI	rs786205001
Exac	rs786205001
Gnomad	rs786205001
Varsome	rs786205001
LitVar	rs786205001
Map	rs786205001
PheGenI	rs786205001
Biobank	rs786205001
1000 genomes	rs786205001
hgdp	rs786205001
ensembl	rs786205001
geneview	rs786205001
scholar	rs786205001
google	rs786205001
pharmgkb	rs786205001
gwascentral	rs786205001
openSNP	rs786205001
23andMe	rs786205001
SNPshot	rs786205001
SNPdbe	rs786205001
MSV3d	rs786205001
GWAS Ctlg	rs786205001

Max Magnitude

0

ClinVar
Risk	rs786205001(-;-)
Alt	rs786205001(-;-)
Reference	Rs786205001(C;C)
Significance	Pathogenic
Disease	Rett syndrome not provided
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant not provided
Reversed	0
HGVS	NC_000014.8:g.29236741delC
CLNSRC
CLNACC	RCV000170073.2, RCV000187475.1,