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rs863224857

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224857(C;T)
Make rs863224857(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position21415880
GeneCHD8
is asnp
is mentioned by
dbSNPrs863224857
ebirs863224857
HLIrs863224857
Exacrs863224857
Varsomers863224857
Maprs863224857
PheGenIrs863224857
hapmaprs863224857
1000 genomesrs863224857
hgdprs863224857
ensemblrs863224857
gopubmedrs863224857
geneviewrs863224857
scholarrs863224857
googlers863224857
pharmgkbrs863224857
gwascentralrs863224857
openSNPrs863224857
23andMers863224857
23andMe allrs863224857
SNP Nexus

SNPshotrs863224857
SNPdbers863224857
MSV3drs863224857
GWAS Ctlgrs863224857
Max Magnitude0
ClinVar
Risk rs863224857(T;T)
Alt rs863224857(T;T)
Reference rs863224857(C;C)
Significance Probable-Pathogenic
Disease Autism
Variation info
Gene CHD8
CLNDBN Autism, susceptibility to, 18
Reversed 1
HGVS NC_000014.8:g.21884039G>A
CLNSRC
CLNACC RCV000197443.1,