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rs886039692

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs886039692(-;-)
Make rs886039692(-;A)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position21409870
GeneCHD8
is asnp
is mentioned by
dbSNPrs886039692
dbSNP (classic)rs886039692
ClinGenrs886039692
ebirs886039692
HLIrs886039692
Exacrs886039692
Gnomadrs886039692
Varsomers886039692
LitVarrs886039692
Maprs886039692
PheGenIrs886039692
Biobankrs886039692
1000 genomesrs886039692
hgdprs886039692
ensemblrs886039692
geneviewrs886039692
scholarrs886039692
googlers886039692
pharmgkbrs886039692
gwascentralrs886039692
openSNPrs886039692
23andMers886039692
23andMe allrs886039692
SNPshotrs886039692
SNPdbers886039692
MSV3drs886039692
GWAS Ctlgrs886039692
Max Magnitude0
ClinVar
Risk rs886039692(-;-)
Alt rs886039692(-;-)
Reference Rs886039692(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21878029delT
CLNSRC
CLNACC RCV000255911.1,