rs869025203

Orientation

minus

Stabilized

minus

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

Make rs869025203(C;T)

Make rs869025203(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

70972667

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs869025203
dbSNP (classic)	rs869025203
ClinGen	rs869025203
ebi	rs869025203
HLI	rs869025203
Exac	rs869025203
Gnomad	rs869025203
Varsome	rs869025203
LitVar	rs869025203
Map	rs869025203
PheGenI	rs869025203
Biobank	rs869025203
1000 genomes	rs869025203
hgdp	rs869025203
ensembl	rs869025203
geneview	rs869025203
scholar	rs869025203
google	rs869025203
pharmgkb	rs869025203
gwascentral	rs869025203
openSNP	rs869025203
23andMe	rs869025203
SNPshot	rs869025203
SNPdbe	rs869025203
MSV3d	rs869025203
GWAS Ctlg	rs869025203

Max Magnitude

0

ClinVar
Risk	rs869025203(T;T)
Alt	rs869025203(T;T)
Reference	Rs869025203(C;C)
Significance	Pathogenic
Disease	Mental retardation with language impairment and with or without autistic features
Variation	info
Gene	FOXP1
CLNDBN	Mental retardation with language impairment and with or without autistic features
Reversed	1
HGVS	NC_000003.11:g.71021818G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000207490.1,