rs587783642

Orientation

plus

Stabilized

plus

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

Make rs587783642(C;G)

Make rs587783642(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

28768041

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs587783642
dbSNP (classic)	rs587783642
ClinGen	rs587783642
ebi	rs587783642
HLI	rs587783642
Exac	rs587783642
Gnomad	rs587783642
Varsome	rs587783642
LitVar	rs587783642
Map	rs587783642
PheGenI	rs587783642
Biobank	rs587783642
1000 genomes	rs587783642
hgdp	rs587783642
ensembl	rs587783642
geneview	rs587783642
scholar	rs587783642
google	rs587783642
pharmgkb	rs587783642
gwascentral	rs587783642
openSNP	rs587783642
23andMe	rs587783642
SNPshot	rs587783642
SNPdbe	rs587783642
MSV3d	rs587783642
GWAS Ctlg	rs587783642

Max Magnitude

0

ClinVar
Risk	rs587783642(G;G)
Alt	rs587783642(G;G)
Reference	Rs587783642(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant
Reversed	0
HGVS	NC_000014.8:g.29237247C>G
CLNSRC
CLNACC	RCV000145996.1,