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

rs1064796255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60828807
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064796255
dbSNP (old)rs1064796255
ClinGenrs1064796255
ebirs1064796255
HLIrs1064796255
Exacrs1064796255
Varsomers1064796255
Maprs1064796255
PheGenIrs1064796255
Biobankrs1064796255
1000 genomesrs1064796255
hgdprs1064796255
ensemblrs1064796255
gopubmedrs1064796255
geneviewrs1064796255
scholarrs1064796255
googlers1064796255
pharmgkbrs1064796255
gwascentralrs1064796255
openSNPrs1064796255
23andMers1064796255
23andMe allrs1064796255
SNP Nexus

SNPshotrs1064796255
SNPdbers1064796255
MSV3drs1064796255
GWAS Ctlgrs1064796255
Max Magnitude0
ClinVar
Risk rs1064796255(-;-)
Alt rs1064796255(-;-)
Reference Rs1064796255(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61741366delG
CLNSRC
CLNACC RCV000478057.1,