rs886039692

Orientation

minus

Stabilized

minus

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

Make rs886039692(-;-)

Make rs886039692(-;A)

Reference

GRCh38.p7 38.3/149

Chromosome

14

Position

21409870

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs886039692
dbSNP (classic)	rs886039692
ClinGen	rs886039692
ebi	rs886039692
HLI	rs886039692
Exac	rs886039692
Gnomad	rs886039692
Varsome	rs886039692
LitVar	rs886039692
Map	rs886039692
PheGenI	rs886039692
Biobank	rs886039692
1000 genomes	rs886039692
hgdp	rs886039692
ensembl	rs886039692
geneview	rs886039692
scholar	rs886039692
google	rs886039692
pharmgkb	rs886039692
gwascentral	rs886039692
openSNP	rs886039692
23andMe	rs886039692
SNPshot	rs886039692
SNPdbe	rs886039692
MSV3d	rs886039692
GWAS Ctlg	rs886039692

Max Magnitude

0

ClinVar
Risk	rs886039692(-;-)
Alt	rs886039692(-;-)
Reference	Rs886039692(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.21878029delT
CLNSRC
CLNACC	RCV000255911.1,