rs267606826

Orientation

plus

Stabilized

plus

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

Make rs267606826(C;G)

Make rs267606826(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

28767903

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs267606826
dbSNP (classic)	rs267606826
ClinGen	rs267606826
ebi	rs267606826
HLI	rs267606826
Exac	rs267606826
Gnomad	rs267606826
Varsome	rs267606826
LitVar	rs267606826
Map	rs267606826
PheGenI	rs267606826
Biobank	rs267606826
1000 genomes	rs267606826
hgdp	rs267606826
ensembl	rs267606826
geneview	rs267606826
scholar	rs267606826
google	rs267606826
pharmgkb	rs267606826
gwascentral	rs267606826
openSNP	rs267606826
23andMe	rs267606826
SNPshot	rs267606826
SNPdbe	rs267606826
MSV3d	rs267606826
GWAS Ctlg	rs267606826

Max Magnitude

0

ClinVar
Risk	rs267606826(G;G) rs267606826(T;T)
Alt	rs267606826(G;G) rs267606826(T;T)
Reference	Rs267606826(C;C)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant
Reversed	0
HGVS	NC_000014.8:g.29237109C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014883.25,