rs794727436

Orientation

minus

Stabilized

minus

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

Make rs794727436(A;A)

Make rs794727436(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

21395816

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs794727436
dbSNP (classic)	rs794727436
ClinGen	rs794727436
ebi	rs794727436
HLI	rs794727436
Exac	rs794727436
Gnomad	rs794727436
Varsome	rs794727436
LitVar	rs794727436
Map	rs794727436
PheGenI	rs794727436
Biobank	rs794727436
1000 genomes	rs794727436
hgdp	rs794727436
ensembl	rs794727436
geneview	rs794727436
scholar	rs794727436
google	rs794727436
pharmgkb	rs794727436
gwascentral	rs794727436
openSNP	rs794727436
23andMe	rs794727436
SNPshot	rs794727436
SNPdbe	rs794727436
MSV3d	rs794727436
GWAS Ctlg	rs794727436

Max Magnitude

0

ClinVar
Risk	rs794727436(A;A)
Alt	rs794727436(A;A)
Reference	Rs794727436(G;G)
Significance	Probable-Pathogenic
Disease	Autism
Variation	info
Gene	CHD8
CLNDBN	Autism, susceptibility to, 18
Reversed	1
HGVS	NC_000014.8:g.21863975C>T
CLNSRC
CLNACC	RCV000176725.1,