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rs776631057

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776631057(A;A)
Make rs776631057(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position21409898
GeneCHD8
is asnp
is mentioned by
dbSNPrs776631057
ebirs776631057
HLIrs776631057
Exacrs776631057
Varsomers776631057
Maprs776631057
PheGenIrs776631057
hapmaprs776631057
1000 genomesrs776631057
hgdprs776631057
ensemblrs776631057
gopubmedrs776631057
geneviewrs776631057
scholarrs776631057
googlers776631057
pharmgkbrs776631057
gwascentralrs776631057
openSNPrs776631057
23andMers776631057
23andMe allrs776631057
SNP Nexus

SNPshotrs776631057
SNPdbers776631057
MSV3drs776631057
GWAS Ctlgrs776631057
Max Magnitude0
ClinVar
Risk rs776631057(A,C;A,C)
Alt rs776631057(A,C;A,C)
Reference rs776631057(G;G)
Significance Probable-Pathogenic
Disease Autism
Variation info
Gene CHD8
CLNDBN Autism, susceptibility to, 18
Reversed 0
HGVS NC_000014.8:g.21878057G>A
CLNSRC
CLNACC RCV000200678.1,