rs869025202

Orientation

minus

Stabilized

minus

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

Make rs869025202(A;G)

Make rs869025202(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

70977678

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs869025202
dbSNP (classic)	rs869025202
ClinGen	rs869025202
ebi	rs869025202
HLI	rs869025202
Exac	rs869025202
Gnomad	rs869025202
Varsome	rs869025202
LitVar	rs869025202
Map	rs869025202
PheGenI	rs869025202
Biobank	rs869025202
1000 genomes	rs869025202
hgdp	rs869025202
ensembl	rs869025202
geneview	rs869025202
scholar	rs869025202
google	rs869025202
pharmgkb	rs869025202
gwascentral	rs869025202
openSNP	rs869025202
23andMe	rs869025202
SNPshot	rs869025202
SNPdbe	rs869025202
MSV3d	rs869025202
GWAS Ctlg	rs869025202

Max Magnitude

0

ClinVar
Risk	rs869025202(G;G)
Alt	rs869025202(G;G)
Reference	Rs869025202(A;A)
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.71026829T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000207489.1,