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rs886041968

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position21405780
GeneCHD8
is asnp
is mentioned by
dbSNPrs886041968
dbSNP (classic)rs886041968
ClinGenrs886041968
ebirs886041968
HLIrs886041968
Exacrs886041968
Gnomadrs886041968
Varsomers886041968
LitVarrs886041968
Maprs886041968
PheGenIrs886041968
Biobankrs886041968
1000 genomesrs886041968
hgdprs886041968
ensemblrs886041968
geneviewrs886041968
scholarrs886041968
googlers886041968
pharmgkbrs886041968
gwascentralrs886041968
openSNPrs886041968
23andMers886041968
23andMe allrs886041968
SNPshotrs886041968
SNPdbers886041968
MSV3drs886041968
GWAS Ctlgrs886041968
Max Magnitude0
ClinVar
Risk rs886041968(T;T)
Alt rs886041968(T;T)
Reference Rs886041968(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21873939G>A
CLNSRC
CLNACC RCV000338868.1,