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rs794727298

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727298(C;T)
Make rs794727298(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60742897
GeneCHD7
is asnp
is mentioned by
dbSNPrs794727298
ebirs794727298
HLIrs794727298
Exacrs794727298
Varsomers794727298
Maprs794727298
PheGenIrs794727298
hapmaprs794727298
1000 genomesrs794727298
hgdprs794727298
ensemblrs794727298
gopubmedrs794727298
geneviewrs794727298
scholarrs794727298
googlers794727298
pharmgkbrs794727298
gwascentralrs794727298
openSNPrs794727298
23andMers794727298
23andMe allrs794727298
SNP Nexus

SNPshotrs794727298
SNPdbers794727298
MSV3drs794727298
GWAS Ctlgrs794727298
Max Magnitude0
ClinVar
Risk rs794727298(T;T)
Alt rs794727298(T;T)
Reference rs794727298(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61655456C>T
CLNSRC
CLNACC RCV000175896.1,