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rs797045469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045469(-;G)
Make rs797045469(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60851292
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045469
ClinGenrs797045469
ebirs797045469
HLIrs797045469
Exacrs797045469
Varsomers797045469
Maprs797045469
PheGenIrs797045469
hapmaprs797045469
1000 genomesrs797045469
hgdprs797045469
ensemblrs797045469
gopubmedrs797045469
geneviewrs797045469
scholarrs797045469
googlers797045469
pharmgkbrs797045469
gwascentralrs797045469
openSNPrs797045469
23andMers797045469
23andMe allrs797045469
SNP Nexus

SNPshotrs797045469
SNPdbers797045469
MSV3drs797045469
GWAS Ctlgrs797045469
Max Magnitude0
ClinVar
Risk rs797045469(G;G)
Alt rs797045469(G;G)
Reference Rs797045469(-;-)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61763851dupG
CLNSRC
CLNACC RCV000195102.1,