rs776631057

Orientation

plus

Stabilized

plus

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

Make rs776631057(A;A)

Make rs776631057(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

21409898

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs776631057
dbSNP (classic)	rs776631057
ClinGen	rs776631057
ebi	rs776631057
HLI	rs776631057
Exac	rs776631057
Gnomad	rs776631057
Varsome	rs776631057
LitVar	rs776631057
Map	rs776631057
PheGenI	rs776631057
Biobank	rs776631057
1000 genomes	rs776631057
hgdp	rs776631057
ensembl	rs776631057
geneview	rs776631057
scholar	rs776631057
google	rs776631057
pharmgkb	rs776631057
gwascentral	rs776631057
openSNP	rs776631057
23andMe	rs776631057
SNPshot	rs776631057
SNPdbe	rs776631057
MSV3d	rs776631057
GWAS Ctlg	rs776631057

Max Magnitude

0

ClinVar
Risk	rs776631057(A;A) rs776631057(C;C)
Alt	rs776631057(A;A) rs776631057(C;C)
Reference	Rs776631057(G;G)
Significance	Probable-Pathogenic
Disease	Autism
Variation	info
Gene	CHD8
CLNDBN	Autism, susceptibility to, 18
Reversed	0
HGVS	NC_000014.8:g.21878057G>A
CLNSRC
CLNACC	RCV000200678.1,