rs797044652

Orientation

minus

Stabilized

minus

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

Make rs797044652(-;C)

Make rs797044652(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

70977935

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs797044652
dbSNP (classic)	rs797044652
ClinGen	rs797044652
ebi	rs797044652
HLI	rs797044652
Exac	rs797044652
Gnomad	rs797044652
Varsome	rs797044652
LitVar	rs797044652
Map	rs797044652
PheGenI	rs797044652
Biobank	rs797044652
1000 genomes	rs797044652
hgdp	rs797044652
ensembl	rs797044652
geneview	rs797044652
scholar	rs797044652
google	rs797044652
pharmgkb	rs797044652
gwascentral	rs797044652
openSNP	rs797044652
23andMe	rs797044652
SNPshot	rs797044652
SNPdbe	rs797044652
MSV3d	rs797044652
GWAS Ctlg	rs797044652

Max Magnitude

0

ClinVar
Risk	rs797044652(C;C)
Alt	rs797044652(C;C)
Reference	Rs797044652(-;-)
Significance	Pathogenic
Disease	Mental retardation with language impairment and with or without autistic features not provided
Variation	info
Gene	FOXP1
CLNDBN	Mental retardation with language impairment and with or without autistic features not provided
Reversed	1
HGVS	NC_000003.11:g.71027087dupG
CLNSRC
CLNACC	RCV000174957.1, RCV000352326.1,