rs769448730

Orientation

plus

Stabilized

plus

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

Make rs769448730(C;C)

Make rs769448730(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

3

Position

70977662

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs769448730
dbSNP (classic)	rs769448730
ClinGen	rs769448730
ebi	rs769448730
HLI	rs769448730
Exac	rs769448730
Gnomad	rs769448730
Varsome	rs769448730
LitVar	rs769448730
Map	rs769448730
PheGenI	rs769448730
Biobank	rs769448730
1000 genomes	rs769448730
hgdp	rs769448730
ensembl	rs769448730
geneview	rs769448730
scholar	rs769448730
google	rs769448730
pharmgkb	rs769448730
gwascentral	rs769448730
openSNP	rs769448730
23andMe	rs769448730
SNPshot	rs769448730
SNPdbe	rs769448730
MSV3d	rs769448730
GWAS Ctlg	rs769448730

Max Magnitude

0

ClinVar
Risk	rs769448730(C;C)
Alt	rs769448730(C;C)
Reference	Rs769448730(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXP1
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.71026813T>C
CLNSRC
CLNACC	RCV000283441.1,