rs766476648

Orientation

plus

Stabilized

plus

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

Make rs766476648(A;C)

Make rs766476648(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

114663469

Gene

FOXP2

is a	snp
is	mentioned by
dbSNP	rs766476648
dbSNP (classic)	rs766476648
ClinGen	rs766476648
ebi	rs766476648
HLI	rs766476648
Exac	rs766476648
Gnomad	rs766476648
Varsome	rs766476648
LitVar	rs766476648
Map	rs766476648
PheGenI	rs766476648
Biobank	rs766476648
1000 genomes	rs766476648
hgdp	rs766476648
ensembl	rs766476648
geneview	rs766476648
scholar	rs766476648
google	rs766476648
pharmgkb	rs766476648
gwascentral	rs766476648
openSNP	rs766476648
23andMe	rs766476648
SNPshot	rs766476648
SNPdbe	rs766476648
MSV3d	rs766476648
GWAS Ctlg	rs766476648

Max Magnitude

0

ClinVar
Risk	rs766476648(C;C)
Alt	rs766476648(C;C)
Reference	Rs766476648(A;A)
Significance	Other
Disease	Speech-language disorder 1
Variation	info
Gene	FOXP2
CLNDBN	Speech-language disorder 1
Reversed	0
HGVS	NC_000007.13:g.114303524A>C
CLNSRC
CLNACC	RCV000234955.2,