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rs1064793909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position60741639
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793909
dbSNP (old)rs1064793909
ClinGenrs1064793909
ebirs1064793909
HLIrs1064793909
Exacrs1064793909
Gnomadrs1064793909
Varsomers1064793909
LitVarrs1064793909
Maprs1064793909
PheGenIrs1064793909
Biobankrs1064793909
1000 genomesrs1064793909
hgdprs1064793909
ensemblrs1064793909
gopubmedrs1064793909
geneviewrs1064793909
scholarrs1064793909
googlers1064793909
pharmgkbrs1064793909
gwascentralrs1064793909
openSNPrs1064793909
23andMers1064793909
23andMe allrs1064793909
SNPshotrs1064793909
SNPdbers1064793909
MSV3drs1064793909
GWAS Ctlgrs1064793909
Max Magnitude0
ClinVar
Risk rs1064793909(-;-)
Alt rs1064793909(-;-)
Reference Rs1064793909(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61654198delT
CLNSRC
CLNACC RCV000481309.1,