rs267606827

Orientation

plus

Stabilized

plus

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

Make rs267606827(A;A)

Make rs267606827(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

28768203

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs267606827
dbSNP (classic)	rs267606827
ClinGen	rs267606827
ebi	rs267606827
HLI	rs267606827
Exac	rs267606827
Gnomad	rs267606827
Varsome	rs267606827
LitVar	rs267606827
Map	rs267606827
PheGenI	rs267606827
Biobank	rs267606827
1000 genomes	rs267606827
hgdp	rs267606827
ensembl	rs267606827
geneview	rs267606827
scholar	rs267606827
google	rs267606827
pharmgkb	rs267606827
gwascentral	rs267606827
openSNP	rs267606827
23andMe	rs267606827
SNPshot	rs267606827
SNPdbe	rs267606827
MSV3d	rs267606827
GWAS Ctlg	rs267606827

Max Magnitude

0

ClinVar
Risk	rs267606827(A;A)
Alt	rs267606827(A;A)
Reference	Rs267606827(G;G)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant
Reversed	0
HGVS	NC_000014.8:g.29237409G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014885.26,