rs869312717

Orientation

plus

Stabilized

plus

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

Make rs869312717(-;-)

Make rs869312717(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

28767733

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs869312717
dbSNP (classic)	rs869312717
ClinGen	rs869312717
ebi	rs869312717
HLI	rs869312717
Exac	rs869312717
Gnomad	rs869312717
Varsome	rs869312717
LitVar	rs869312717
Map	rs869312717
PheGenI	rs869312717
Biobank	rs869312717
1000 genomes	rs869312717
hgdp	rs869312717
ensembl	rs869312717
geneview	rs869312717
scholar	rs869312717
google	rs869312717
pharmgkb	rs869312717
gwascentral	rs869312717
openSNP	rs869312717
23andMe	rs869312717
SNPshot	rs869312717
SNPdbe	rs869312717
MSV3d	rs869312717
GWAS Ctlg	rs869312717

Max Magnitude

0

ClinVar
Risk	rs869312717(-;-)
Alt	rs869312717(-;-)
Reference	Rs869312717(G;G)
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.29236945delG
CLNSRC
CLNACC	RCV000209851.1, RCV000414502.1,