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rs781575717

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781575717(G;T)
Make rs781575717(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position21392760
GeneCHD8, SNORD9
is asnp
is mentioned by
dbSNPrs781575717
dbSNP (classic)rs781575717
ClinGenrs781575717
ebirs781575717
HLIrs781575717
Exacrs781575717
Gnomadrs781575717
Varsomers781575717
LitVarrs781575717
Maprs781575717
PheGenIrs781575717
Biobankrs781575717
1000 genomesrs781575717
hgdprs781575717
ensemblrs781575717
geneviewrs781575717
scholarrs781575717
googlers781575717
pharmgkbrs781575717
gwascentralrs781575717
openSNPrs781575717
23andMers781575717
23andMe allrs781575717
SNPshotrs781575717
SNPdbers781575717
MSV3drs781575717
GWAS Ctlgrs781575717
Max Magnitude0
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,