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rs794727436

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727436(A;A)
Make rs794727436(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position21395816
GeneCHD8
is asnp
is mentioned by
dbSNPrs794727436
ebirs794727436
HLIrs794727436
Exacrs794727436
Varsomers794727436
Maprs794727436
PheGenIrs794727436
hapmaprs794727436
1000 genomesrs794727436
hgdprs794727436
ensemblrs794727436
gopubmedrs794727436
geneviewrs794727436
scholarrs794727436
googlers794727436
pharmgkbrs794727436
gwascentralrs794727436
openSNPrs794727436
23andMers794727436
23andMe allrs794727436
SNP Nexus

SNPshotrs794727436
SNPdbers794727436
MSV3drs794727436
GWAS Ctlgrs794727436
Max Magnitude0
ClinVar
Risk rs794727436(A;A)
Alt rs794727436(A;A)
Reference rs794727436(G;G)
Significance Probable-Pathogenic
Disease Autism
Variation info
Gene CHD8
CLNDBN Autism, susceptibility to, 18
Reversed 1
HGVS NC_000014.8:g.21863975C>T
CLNSRC
CLNACC RCV000176725.1,