rs863224857

Orientation

minus

Stabilized

minus

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

Make rs863224857(C;T)

Make rs863224857(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

21415880

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs863224857
dbSNP (classic)	rs863224857
ClinGen	rs863224857
ebi	rs863224857
HLI	rs863224857
Exac	rs863224857
Gnomad	rs863224857
Varsome	rs863224857
LitVar	rs863224857
Map	rs863224857
PheGenI	rs863224857
Biobank	rs863224857
1000 genomes	rs863224857
hgdp	rs863224857
ensembl	rs863224857
geneview	rs863224857
scholar	rs863224857
google	rs863224857
pharmgkb	rs863224857
gwascentral	rs863224857
openSNP	rs863224857
23andMe	rs863224857
SNPshot	rs863224857
SNPdbe	rs863224857
MSV3d	rs863224857
GWAS Ctlg	rs863224857

Max Magnitude

0

ClinVar
Risk	rs863224857(T;T)
Alt	rs863224857(T;T)
Reference	Rs863224857(C;C)
Significance	Probable-Pathogenic
Disease	Autism
Variation	info
Gene	CHD8
CLNDBN	Autism, susceptibility to, 18
Reversed	1
HGVS	NC_000014.8:g.21884039G>A
CLNSRC
CLNACC	RCV000197443.1,