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rs797045465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045465(-;A)
Make rs797045465(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60820035
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045465
dbSNP (old)rs797045465
ClinGenrs797045465
ebirs797045465
HLIrs797045465
Exacrs797045465
Varsomers797045465
Maprs797045465
PheGenIrs797045465
Biobankrs797045465
1000 genomesrs797045465
hgdprs797045465
ensemblrs797045465
gopubmedrs797045465
geneviewrs797045465
scholarrs797045465
googlers797045465
pharmgkbrs797045465
gwascentralrs797045465
openSNPrs797045465
23andMers797045465
23andMe allrs797045465
SNP Nexus

SNPshotrs797045465
SNPdbers797045465
MSV3drs797045465
GWAS Ctlgrs797045465
Max Magnitude0
ClinVar
Risk rs797045465(A;A)
Alt rs797045465(A;A)
Reference Rs797045465(-;-)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61732594dupA
CLNSRC
CLNACC RCV000192729.1,