rs1057518999

Orientation

minus

Stabilized

minus

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

Make rs1057518999(C;C)

Make rs1057518999(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

70977826

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs1057518999
dbSNP (classic)	rs1057518999
ClinGen	rs1057518999
ebi	rs1057518999
HLI	rs1057518999
Exac	rs1057518999
Gnomad	rs1057518999
Varsome	rs1057518999
LitVar	rs1057518999
Map	rs1057518999
PheGenI	rs1057518999
Biobank	rs1057518999
1000 genomes	rs1057518999
hgdp	rs1057518999
ensembl	rs1057518999
geneview	rs1057518999
scholar	rs1057518999
google	rs1057518999
pharmgkb	rs1057518999
gwascentral	rs1057518999
openSNP	rs1057518999
23andMe	rs1057518999
SNPshot	rs1057518999
SNPdbe	rs1057518999
MSV3d	rs1057518999
GWAS Ctlg	rs1057518999

Max Magnitude

0

ClinVar
Risk	rs1057518999(C;C)
Alt	rs1057518999(C;C)
Reference	Rs1057518999(T;T)
Significance	Probable-Pathogenic
Disease	Autism
Variation	info
Gene	FOXP1
CLNDBN	Autism
Reversed	1
HGVS	NC_000003.11:g.71026977A>G
CLNSRC
CLNACC	RCV000414900.1,