rs781575717

Orientation

plus

Stabilized

plus

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

Make rs781575717(G;T)

Make rs781575717(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

21392760

Gene	CHD8, SNORD9

is a	snp
is	mentioned by
dbSNP	rs781575717
dbSNP (classic)	rs781575717
ClinGen	rs781575717
ebi	rs781575717
HLI	rs781575717
Exac	rs781575717
Gnomad	rs781575717
Varsome	rs781575717
LitVar	rs781575717
Map	rs781575717
PheGenI	rs781575717
Biobank	rs781575717
1000 genomes	rs781575717
hgdp	rs781575717
ensembl	rs781575717
geneview	rs781575717
scholar	rs781575717
google	rs781575717
pharmgkb	rs781575717
gwascentral	rs781575717
openSNP	rs781575717
23andMe	rs781575717
SNPshot	rs781575717
SNPdbe	rs781575717
MSV3d	rs781575717
GWAS Ctlg	rs781575717

Max Magnitude

0

ClinVar
Risk	rs781575717(A;A) rs781575717(T;T)
Alt	rs781575717(A;A) rs781575717(T;T)
Reference	Rs781575717(G;G)
Significance	Pathogenic
Disease	Autism
Variation	info
Gene	CHD8 SNORD9
CLNDBN	Autism, susceptibility to, 18
Reversed	0
HGVS	NC_000014.8:g.21860919G>T
CLNSRC
CLNACC	RCV000414935.1,