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rs886039725

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCTTCATAG;TCTTCATAG) 0 common in clinvar
Make rs886039725(-;-)
Make rs886039725(-;TCTTCATAG)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position21401072
GeneCHD8
is asnp
is mentioned by
dbSNPrs886039725
dbSNP (classic)rs886039725
ClinGenrs886039725
ebirs886039725
HLIrs886039725
Exacrs886039725
Gnomadrs886039725
Varsomers886039725
LitVarrs886039725
Maprs886039725
PheGenIrs886039725
Biobankrs886039725
1000 genomesrs886039725
hgdprs886039725
ensemblrs886039725
geneviewrs886039725
scholarrs886039725
googlers886039725
pharmgkbrs886039725
gwascentralrs886039725
openSNPrs886039725
23andMers886039725
23andMe allrs886039725
SNPshotrs886039725
SNPdbers886039725
MSV3drs886039725
GWAS Ctlgrs886039725
Max Magnitude0
ClinVar
Risk rs886039725(-;-)
Alt rs886039725(-;-)
Reference Rs886039725(TCTTCATAG;TCTTCATAG)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21869231_21869239delCTATGAAGA
CLNSRC
CLNACC RCV000255702.1,