rs786200976

Orientation

plus

Stabilized

plus

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

Make rs786200976(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

114631608

Gene

FOXP2

is a	snp
is	mentioned by
dbSNP	rs786200976
dbSNP (classic)	rs786200976
ClinGen	rs786200976
ebi	rs786200976
HLI	rs786200976
Exac	rs786200976
Gnomad	rs786200976
Varsome	rs786200976
LitVar	rs786200976
Map	rs786200976
PheGenI	rs786200976
Biobank	rs786200976
1000 genomes	rs786200976
hgdp	rs786200976
ensembl	rs786200976
geneview	rs786200976
scholar	rs786200976
google	rs786200976
pharmgkb	rs786200976
gwascentral	rs786200976
openSNP	rs786200976
23andMe	rs786200976
SNPshot	rs786200976
SNPdbe	rs786200976
MSV3d	rs786200976
GWAS Ctlg	rs786200976

Max Magnitude

3

aka c.678dupA (p.Leu227Thrfs)

ClinVar
Risk	rs786200976(A;A)
Alt	rs786200976(A;A)
Reference	Rs786200976(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.114271663dupA
CLNSRC
CLNACC	RCV000153269.3,