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rs797045467

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045467(C;T)
Make rs797045467(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60845036
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045467
ebirs797045467
HLIrs797045467
Exacrs797045467
Varsomers797045467
Maprs797045467
PheGenIrs797045467
hapmaprs797045467
1000 genomesrs797045467
hgdprs797045467
ensemblrs797045467
gopubmedrs797045467
geneviewrs797045467
scholarrs797045467
googlers797045467
pharmgkbrs797045467
gwascentralrs797045467
openSNPrs797045467
23andMers797045467
23andMe allrs797045467
SNP Nexus

SNPshotrs797045467
SNPdbers797045467
MSV3drs797045467
GWAS Ctlgrs797045467
Max Magnitude0
ClinVar
Risk rs797045467(T;T)
Alt rs797045467(T;T)
Reference rs797045467(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61757595C>T
CLNSRC
CLNACC RCV000192854.1,