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rs1085307794

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position21394976
GeneCHD8
is asnp
is mentioned by
dbSNPrs1085307794
dbSNP (old)rs1085307794
ClinGenrs1085307794
ebirs1085307794
HLIrs1085307794
Exacrs1085307794
Gnomadrs1085307794
Varsomers1085307794
Maprs1085307794
PheGenIrs1085307794
Biobankrs1085307794
1000 genomesrs1085307794
hgdprs1085307794
ensemblrs1085307794
gopubmedrs1085307794
geneviewrs1085307794
scholarrs1085307794
googlers1085307794
pharmgkbrs1085307794
gwascentralrs1085307794
openSNPrs1085307794
23andMers1085307794
23andMe allrs1085307794
SNPshotrs1085307794
SNPdbers1085307794
MSV3drs1085307794
GWAS Ctlgrs1085307794
Max Magnitude0
ClinVar
Risk rs1085307794(T;T)
Alt rs1085307794(T;T)
Reference Rs1085307794(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21863135G>A
CLNSRC
CLNACC RCV000490191.1,