rs1064796666

Orientation

minus

Stabilized

minus

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

Chromosome

14

Position

21391581

Gene	CHD8, LOC107984643

is a	snp
is	mentioned by
dbSNP	rs1064796666
dbSNP (classic)	rs1064796666
ClinGen	rs1064796666
ebi	rs1064796666
HLI	rs1064796666
Exac	rs1064796666
Gnomad	rs1064796666
Varsome	rs1064796666
LitVar	rs1064796666
Map	rs1064796666
PheGenI	rs1064796666
Biobank	rs1064796666
1000 genomes	rs1064796666
hgdp	rs1064796666
ensembl	rs1064796666
geneview	rs1064796666
scholar	rs1064796666
google	rs1064796666
pharmgkb	rs1064796666
gwascentral	rs1064796666
openSNP	rs1064796666
23andMe	rs1064796666
SNPshot	rs1064796666
SNPdbe	rs1064796666
MSV3d	rs1064796666
GWAS Ctlg	rs1064796666

Max Magnitude

0

ClinVar
Risk	rs1064796666(-;-)
Alt	rs1064796666(-;-)
Reference	Rs1064796666(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.21859740delG
CLNSRC
CLNACC	RCV000481022.1,