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rs1064795655

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position21403663
GeneCHD8
is asnp
is mentioned by
dbSNPrs1064795655
dbSNP (old)rs1064795655
ClinGenrs1064795655
ebirs1064795655
HLIrs1064795655
Exacrs1064795655
Gnomadrs1064795655
Varsomers1064795655
Maprs1064795655
PheGenIrs1064795655
Biobankrs1064795655
1000 genomesrs1064795655
hgdprs1064795655
ensemblrs1064795655
gopubmedrs1064795655
geneviewrs1064795655
scholarrs1064795655
googlers1064795655
pharmgkbrs1064795655
gwascentralrs1064795655
openSNPrs1064795655
23andMers1064795655
23andMe allrs1064795655
SNPshotrs1064795655
SNPdbers1064795655
MSV3drs1064795655
GWAS Ctlgrs1064795655
Max Magnitude0
ClinVar
Risk rs1064795655(T;T)
Alt rs1064795655(T;T)
Reference Rs1064795655(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21871822C>A
CLNSRC
CLNACC RCV000484621.1,