rs786205004

Orientation

plus

Stabilized

plus

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

Make rs786205004(-;C)

Make rs786205004(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767831

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs786205004
dbSNP (classic)	rs786205004
ClinGen	rs786205004
ebi	rs786205004
HLI	rs786205004
Exac	rs786205004
Gnomad	rs786205004
Varsome	rs786205004
LitVar	rs786205004
Map	rs786205004
PheGenI	rs786205004
Biobank	rs786205004
1000 genomes	rs786205004
hgdp	rs786205004
ensembl	rs786205004
geneview	rs786205004
scholar	rs786205004
google	rs786205004
pharmgkb	rs786205004
gwascentral	rs786205004
openSNP	rs786205004
23andMe	rs786205004
SNPshot	rs786205004
SNPdbe	rs786205004
MSV3d	rs786205004
GWAS Ctlg	rs786205004

Max Magnitude

0

ClinVar
Risk	rs786205004(C;C)
Alt	rs786205004(C;C)
Reference	Rs786205004(-;-)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant
Reversed	0
HGVS	NC_000014.8:g.29237037dupC
CLNSRC
CLNACC	RCV000170077.1,