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rs1064796666

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position21391581
GeneCHD8, LOC107984643
is asnp
is mentioned by
dbSNPrs1064796666
dbSNP (old)rs1064796666
ClinGenrs1064796666
ebirs1064796666
HLIrs1064796666
Exacrs1064796666
Gnomadrs1064796666
Varsomers1064796666
Maprs1064796666
PheGenIrs1064796666
Biobankrs1064796666
1000 genomesrs1064796666
hgdprs1064796666
ensemblrs1064796666
gopubmedrs1064796666
geneviewrs1064796666
scholarrs1064796666
googlers1064796666
pharmgkbrs1064796666
gwascentralrs1064796666
openSNPrs1064796666
23andMers1064796666
23andMe allrs1064796666
SNPshotrs1064796666
SNPdbers1064796666
MSV3drs1064796666
GWAS Ctlgrs1064796666
Max Magnitude0
ClinVar
Risk rs1064796666(-;-)
Alt rs1064796666(-;-)
Reference Rs1064796666(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21859740delG
CLNSRC
CLNACC RCV000481022.1,