rs1057518651

Orientation

minus

Stabilized

minus

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

Make rs1057518651(C;T)

Make rs1057518651(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

21408756

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs1057518651
dbSNP (classic)	rs1057518651
ClinGen	rs1057518651
ebi	rs1057518651
HLI	rs1057518651
Exac	rs1057518651
Gnomad	rs1057518651
Varsome	rs1057518651
LitVar	rs1057518651
Map	rs1057518651
PheGenI	rs1057518651
Biobank	rs1057518651
1000 genomes	rs1057518651
hgdp	rs1057518651
ensembl	rs1057518651
geneview	rs1057518651
scholar	rs1057518651
google	rs1057518651
pharmgkb	rs1057518651
gwascentral	rs1057518651
openSNP	rs1057518651
23andMe	rs1057518651
SNPshot	rs1057518651
SNPdbe	rs1057518651
MSV3d	rs1057518651
GWAS Ctlg	rs1057518651

Max Magnitude

0

ClinVar
Risk	rs1057518651(T;T)
Alt	rs1057518651(T;T)
Reference	Rs1057518651(C;C)
Significance	Probable-Pathogenic
Disease	Autism
Variation	info
Gene	CHD8
CLNDBN	Autism, susceptibility to, 18
Reversed	1
HGVS	NC_000014.8:g.21876915G>A
CLNSRC
CLNACC	RCV000414983.1,