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rs1057518651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518651(C;T)
Make rs1057518651(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position21408756
GeneCHD8
is asnp
is mentioned by
dbSNPrs1057518651
dbSNP (old)rs1057518651
ClinGenrs1057518651
ebirs1057518651
HLIrs1057518651
Exacrs1057518651
Gnomadrs1057518651
Varsomers1057518651
Maprs1057518651
PheGenIrs1057518651
Biobankrs1057518651
1000 genomesrs1057518651
hgdprs1057518651
ensemblrs1057518651
gopubmedrs1057518651
geneviewrs1057518651
scholarrs1057518651
googlers1057518651
pharmgkbrs1057518651
gwascentralrs1057518651
openSNPrs1057518651
23andMers1057518651
23andMe allrs1057518651
SNPshotrs1057518651
SNPdbers1057518651
MSV3drs1057518651
GWAS Ctlgrs1057518651
Max Magnitude0
ClinVar
Risk rs1057518651(T;T)
Alt rs1057518651(T;T)
Reference Rs1057518651(C;C)
Significance Probable-Pathogenic
Disease Autism
Variation info
Gene CHD8
CLNDBN Autism, susceptibility to, 18
Reversed 1
HGVS NC_000014.8:g.21876915G>A
CLNSRC
CLNACC RCV000414983.1,