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rs794727569

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727569(A;A)
Make rs794727569(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60856033
GeneCHD7
is asnp
is mentioned by
dbSNPrs794727569
ebirs794727569
HLIrs794727569
Exacrs794727569
Varsomers794727569
Maprs794727569
PheGenIrs794727569
hapmaprs794727569
1000 genomesrs794727569
hgdprs794727569
ensemblrs794727569
gopubmedrs794727569
geneviewrs794727569
scholarrs794727569
googlers794727569
pharmgkbrs794727569
gwascentralrs794727569
openSNPrs794727569
23andMers794727569
23andMe allrs794727569
SNP Nexus

SNPshotrs794727569
SNPdbers794727569
MSV3drs794727569
GWAS Ctlgrs794727569
Max Magnitude0
ClinVar
Risk rs794727569(A;A)
Alt rs794727569(A;A)
Reference rs794727569(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61768592G>A
CLNSRC
CLNACC RCV000177749.1,