rs587783641

Orientation

plus

Stabilized

plus

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

Make rs587783641(A;G)

Make rs587783641(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

28768036

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs587783641
dbSNP (classic)	rs587783641
ClinGen	rs587783641
ebi	rs587783641
HLI	rs587783641
Exac	rs587783641
Gnomad	rs587783641
Varsome	rs587783641
LitVar	rs587783641
Map	rs587783641
PheGenI	rs587783641
Biobank	rs587783641
1000 genomes	rs587783641
hgdp	rs587783641
ensembl	rs587783641
geneview	rs587783641
scholar	rs587783641
google	rs587783641
pharmgkb	rs587783641
gwascentral	rs587783641
openSNP	rs587783641
23andMe	rs587783641
SNPshot	rs587783641
SNPdbe	rs587783641
MSV3d	rs587783641
GWAS Ctlg	rs587783641

Max Magnitude

0

ClinVar
Risk	rs587783641(G;G)
Alt	rs587783641(G;G)
Reference	Rs587783641(A;A)
Significance	Pathogenic
Disease	Rett syndrome
Variation	info
Gene	FOXG1
CLNDBN	Rett syndrome, congenital variant
Reversed	0
HGVS	NC_000014.8:g.29237242A>G
CLNSRC
CLNACC	RCV000145995.2,