rs879253770

Orientation

plus

Stabilized

plus

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

Make rs879253770(ACAACAGCAGCA;ACAACAGCAGCA)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

114629914

Gene

FOXP2

is a	snp
is	mentioned by
dbSNP	rs879253770
dbSNP (classic)	rs879253770
ClinGen	rs879253770
ebi	rs879253770
HLI	rs879253770
Exac	rs879253770
Gnomad	rs879253770
Varsome	rs879253770
LitVar	rs879253770
Map	rs879253770
PheGenI	rs879253770
Biobank	rs879253770
1000 genomes	rs879253770
hgdp	rs879253770
ensembl	rs879253770
geneview	rs879253770
scholar	rs879253770
google	rs879253770
pharmgkb	rs879253770
gwascentral	rs879253770
openSNP	rs879253770
23andMe	rs879253770
SNPshot	rs879253770
SNPdbe	rs879253770
MSV3d	rs879253770
GWAS Ctlg	rs879253770

Max Magnitude

3

ClinVar
Risk	rs879253770(ACAACAGCAGCA;ACAACAGCAGCA) rs879253770(CAGCAGCAACAA;CAGCAGCAACAA)
Alt	rs879253770(ACAACAGCAGCA;ACAACAGCAGCA) rs879253770(CAGCAGCAACAA;CAGCAGCAACAA)
Reference	Rs879253770(-;-)
Significance	Pathogenic
Disease	Speech-language disorder 1
Variation	info
Gene	FOXP2
CLNDBN	Speech-language disorder 1
Reversed	0
HGVS	NC_000007.13:g.114269958_114269969dupACAACAGCAGCA
CLNSRC
CLNACC	RCV000234942.1,