rs886039725

Orientation

minus

Stabilized

minus

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

Make rs886039725(-;-)

Make rs886039725(-;TCTTCATAG)

Reference

GRCh38.p7 38.3/149

Chromosome

14

Position

21401072

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs886039725
dbSNP (classic)	rs886039725
ClinGen	rs886039725
ebi	rs886039725
HLI	rs886039725
Exac	rs886039725
Gnomad	rs886039725
Varsome	rs886039725
LitVar	rs886039725
Map	rs886039725
PheGenI	rs886039725
Biobank	rs886039725
1000 genomes	rs886039725
hgdp	rs886039725
ensembl	rs886039725
geneview	rs886039725
scholar	rs886039725
google	rs886039725
pharmgkb	rs886039725
gwascentral	rs886039725
openSNP	rs886039725
23andMe	rs886039725
SNPshot	rs886039725
SNPdbe	rs886039725
MSV3d	rs886039725
GWAS Ctlg	rs886039725

Max Magnitude

0

ClinVar
Risk	rs886039725(-;-)
Alt	rs886039725(-;-)
Reference	Rs886039725(TCTTCATAG;TCTTCATAG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.21869231_21869239delCTATGAAGA
CLNSRC
CLNACC	RCV000255702.1,