rs879253772

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	3	speech and other processing issues possible
(T;T)	0	common in clinvar

Make rs879253772(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

114659617

Gene

FOXP2

is a	snp
is	mentioned by
dbSNP	rs879253772
dbSNP (classic)	rs879253772
ClinGen	rs879253772
ebi	rs879253772
HLI	rs879253772
Exac	rs879253772
Gnomad	rs879253772
Varsome	rs879253772
LitVar	rs879253772
Map	rs879253772
PheGenI	rs879253772
Biobank	rs879253772
1000 genomes	rs879253772
hgdp	rs879253772
ensembl	rs879253772
geneview	rs879253772
scholar	rs879253772
google	rs879253772
pharmgkb	rs879253772
gwascentral	rs879253772
openSNP	rs879253772
23andMe	rs879253772
SNPshot	rs879253772
SNPdbe	rs879253772
MSV3d	rs879253772
GWAS Ctlg	rs879253772

Max Magnitude

3

ClinVar
Risk	rs879253772(C;C)
Alt	rs879253772(C;C)
Reference	Rs879253772(T;T)
Significance	Pathogenic
Disease	Speech-language disorder 1
Variation	info
Gene	FOXP2
CLNDBN	Speech-language disorder 1
Reversed	0
HGVS	NC_000007.13:g.114299672T>C
CLNSRC
CLNACC	RCV000234952.1,