rs1057518926

Orientation

minus

Stabilized

minus

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

Make rs1057518926(C;G)

Make rs1057518926(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

70977675

Gene

FOXP1

is a	snp
is	mentioned by
dbSNP	rs1057518926
dbSNP (classic)	rs1057518926
ClinGen	rs1057518926
ebi	rs1057518926
HLI	rs1057518926
Exac	rs1057518926
Gnomad	rs1057518926
Varsome	rs1057518926
LitVar	rs1057518926
Map	rs1057518926
PheGenI	rs1057518926
Biobank	rs1057518926
1000 genomes	rs1057518926
hgdp	rs1057518926
ensembl	rs1057518926
geneview	rs1057518926
scholar	rs1057518926
google	rs1057518926
pharmgkb	rs1057518926
gwascentral	rs1057518926
openSNP	rs1057518926
23andMe	rs1057518926
SNPshot	rs1057518926
SNPdbe	rs1057518926
MSV3d	rs1057518926
GWAS Ctlg	rs1057518926

Max Magnitude

0

ClinVar
Risk	rs1057518926(G;G)
Alt	rs1057518926(G;G)
Reference	Rs1057518926(C;C)
Significance	Probable-Pathogenic
Disease	Anterior creases of earlobe Delayed speech and language development Glabellar hemangioma Intellectual disability Strabismus
Variation	info
Gene	FOXP1
CLNDBN	Anterior creases of earlobe Delayed speech and language development Glabellar hemangioma Intellectual disability Strabismus
Reversed	1
HGVS	NC_000003.11:g.71026826G>C
CLNSRC
CLNACC	RCV000414948.1,