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rs797045468

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045468(-;G)
Make rs797045468(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60741960
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045468
ClinGenrs797045468
ebirs797045468
HLIrs797045468
Exacrs797045468
Varsomers797045468
Maprs797045468
PheGenIrs797045468
hapmaprs797045468
1000 genomesrs797045468
hgdprs797045468
ensemblrs797045468
gopubmedrs797045468
geneviewrs797045468
scholarrs797045468
googlers797045468
pharmgkbrs797045468
gwascentralrs797045468
openSNPrs797045468
23andMers797045468
23andMe allrs797045468
SNP Nexus

SNPshotrs797045468
SNPdbers797045468
MSV3drs797045468
GWAS Ctlgrs797045468
Max Magnitude0
ClinVar
Risk rs797045468(G;G)
Alt rs797045468(G;G)
Reference Rs797045468(-;-)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61654519dupG
CLNSRC
CLNACC RCV000193887.1,