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rs886041884

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position21402485
GeneCHD8
is asnp
is mentioned by
dbSNPrs886041884
dbSNP (classic)rs886041884
ClinGenrs886041884
ebirs886041884
HLIrs886041884
Exacrs886041884
Gnomadrs886041884
Varsomers886041884
LitVarrs886041884
Maprs886041884
PheGenIrs886041884
Biobankrs886041884
1000 genomesrs886041884
hgdprs886041884
ensemblrs886041884
geneviewrs886041884
scholarrs886041884
googlers886041884
pharmgkbrs886041884
gwascentralrs886041884
openSNPrs886041884
23andMers886041884
23andMe allrs886041884
SNPshotrs886041884
SNPdbers886041884
MSV3drs886041884
GWAS Ctlgrs886041884
Max Magnitude0
ClinVar
Risk rs886041884(T;T)
Alt rs886041884(T;T)
Reference Rs886041884(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21870644G>A
CLNSRC
CLNACC RCV000388503.1,