Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064796926

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Chromosome8
Position60823864
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064796926
dbSNP (old)rs1064796926
ClinGenrs1064796926
ebirs1064796926
HLIrs1064796926
Exacrs1064796926
Gnomadrs1064796926
Varsomers1064796926
Maprs1064796926
PheGenIrs1064796926
Biobankrs1064796926
1000 genomesrs1064796926
hgdprs1064796926
ensemblrs1064796926
gopubmedrs1064796926
geneviewrs1064796926
scholarrs1064796926
googlers1064796926
pharmgkbrs1064796926
gwascentralrs1064796926
openSNPrs1064796926
23andMers1064796926
23andMe allrs1064796926
SNP Nexus

SNPshotrs1064796926
SNPdbers1064796926
MSV3drs1064796926
GWAS Ctlgrs1064796926
Max Magnitude0
ClinVar
Risk rs1064796926(-;-)
Alt rs1064796926(-;-)
Reference Rs1064796926(AA;AA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61736423_61736424delAA
CLNSRC
CLNACC RCV000483407.1,