rs879253771

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;CA)	3	speech and other processing issues possible
(AC;AC)	0	common in clinvar

Make rs879253771(-;-)

Make rs879253771(CA;CA)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

114652276

Gene	FOXP2, MIR3666

is a	snp
is	mentioned by
dbSNP	rs879253771
dbSNP (classic)	rs879253771
ClinGen	rs879253771
ebi	rs879253771
HLI	rs879253771
Exac	rs879253771
Gnomad	rs879253771
Varsome	rs879253771
LitVar	rs879253771
Map	rs879253771
PheGenI	rs879253771
Biobank	rs879253771
1000 genomes	rs879253771
hgdp	rs879253771
ensembl	rs879253771
geneview	rs879253771
scholar	rs879253771
google	rs879253771
pharmgkb	rs879253771
gwascentral	rs879253771
openSNP	rs879253771
23andMe	rs879253771
SNPshot	rs879253771
SNPdbe	rs879253771
MSV3d	rs879253771
GWAS Ctlg	rs879253771

Max Magnitude

3

ClinVar
Risk	rs879253771(-;-)
Alt	rs879253771(-;-)
Reference	Rs879253771(AC;AC)
Significance	Pathogenic
Disease	Speech-language disorder 1
Variation	info
Gene	FOXP2 MIR3666
CLNDBN	Speech-language disorder 1
Reversed	0
HGVS	NC_000007.13:g.114292331_114292332delCA
CLNSRC
CLNACC	RCV000234941.1,