rs267606828

Orientation

plus

Stabilized

plus

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

Make rs267606828(C;C)

Make rs267606828(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

28767922

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs267606828
dbSNP (classic)	rs267606828
ClinGen	rs267606828
ebi	rs267606828
HLI	rs267606828
Exac	rs267606828
Gnomad	rs267606828
Varsome	rs267606828
LitVar	rs267606828
Map	rs267606828
PheGenI	rs267606828
Biobank	rs267606828
1000 genomes	rs267606828
hgdp	rs267606828
ensembl	rs267606828
geneview	rs267606828
scholar	rs267606828
google	rs267606828
pharmgkb	rs267606828
gwascentral	rs267606828
openSNP	rs267606828
23andMe	rs267606828
SNPshot	rs267606828
SNPdbe	rs267606828
MSV3d	rs267606828
GWAS Ctlg	rs267606828

Max Magnitude

0

ClinVar
Risk	rs267606828(C;C)
Alt	rs267606828(C;C)
Reference	Rs267606828(T;T)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant
Reversed	0
HGVS	NC_000014.8:g.29237128T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014884.26,