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rs1064793346

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position60862244
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793346
dbSNP (old)rs1064793346
ClinGenrs1064793346
ebirs1064793346
HLIrs1064793346
Exacrs1064793346
Gnomadrs1064793346
Varsomers1064793346
Maprs1064793346
PheGenIrs1064793346
Biobankrs1064793346
1000 genomesrs1064793346
hgdprs1064793346
ensemblrs1064793346
gopubmedrs1064793346
geneviewrs1064793346
scholarrs1064793346
googlers1064793346
pharmgkbrs1064793346
gwascentralrs1064793346
openSNPrs1064793346
23andMers1064793346
23andMe allrs1064793346
SNP Nexus

SNPshotrs1064793346
SNPdbers1064793346
MSV3drs1064793346
GWAS Ctlgrs1064793346
Max Magnitude0
ClinVar
Risk rs1064793346(T;T)
Alt rs1064793346(T;T)
Reference Rs1064793346(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61774803C>T
CLNSRC
CLNACC RCV000482183.1,