rs794727155

Orientation

minus

Stabilized

minus

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

Make rs794727155(A;A)

Make rs794727155(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

70977859

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs794727155
dbSNP (classic)	rs794727155
ClinGen	rs794727155
ebi	rs794727155
HLI	rs794727155
Exac	rs794727155
Gnomad	rs794727155
Varsome	rs794727155
LitVar	rs794727155
Map	rs794727155
PheGenI	rs794727155
Biobank	rs794727155
1000 genomes	rs794727155
hgdp	rs794727155
ensembl	rs794727155
geneview	rs794727155
scholar	rs794727155
google	rs794727155
pharmgkb	rs794727155
gwascentral	rs794727155
openSNP	rs794727155
23andMe	rs794727155
SNPshot	rs794727155
SNPdbe	rs794727155
MSV3d	rs794727155
GWAS Ctlg	rs794727155

Max Magnitude

0

ClinVar
Risk	rs794727155(A;A) rs794727155(G;G)
Alt	rs794727155(A;A) rs794727155(G;G)
Reference	Rs794727155(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.71027010G>C; NC_000003.11:g.71027010G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000207487.1, RCV000174956.1,