rs1057524732

Orientation

minus

Stabilized

minus

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

Make rs1057524732(C;T)

Make rs1057524732(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

71047032

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs1057524732
dbSNP (classic)	rs1057524732
ClinGen	rs1057524732
ebi	rs1057524732
HLI	rs1057524732
Exac	rs1057524732
Gnomad	rs1057524732
Varsome	rs1057524732
LitVar	rs1057524732
Map	rs1057524732
PheGenI	rs1057524732
Biobank	rs1057524732
1000 genomes	rs1057524732
hgdp	rs1057524732
ensembl	rs1057524732
geneview	rs1057524732
scholar	rs1057524732
google	rs1057524732
pharmgkb	rs1057524732
gwascentral	rs1057524732
openSNP	rs1057524732
23andMe	rs1057524732
SNPshot	rs1057524732
SNPdbe	rs1057524732
MSV3d	rs1057524732
GWAS Ctlg	rs1057524732

Max Magnitude

0

ClinVar
Risk	rs1057524732(T;T)
Alt	rs1057524732(T;T)
Reference	Rs1057524732(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXP1
CLNDBN	not provided
Reversed	1
HGVS	NC_000003.11:g.71096183G>A
CLNSRC
CLNACC	RCV000429050.1,