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rs587783459

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783459(A;A)
Make rs587783459(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60862631
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783459
ebirs587783459
HLIrs587783459
Exacrs587783459
Varsomers587783459
Maprs587783459
PheGenIrs587783459
hapmaprs587783459
1000 genomesrs587783459
hgdprs587783459
ensemblrs587783459
gopubmedrs587783459
geneviewrs587783459
scholarrs587783459
googlers587783459
pharmgkbrs587783459
gwascentralrs587783459
openSNPrs587783459
23andMers587783459
23andMe allrs587783459
SNP Nexus

SNPshotrs587783459
SNPdbers587783459
MSV3drs587783459
GWAS Ctlgrs587783459
Max Magnitude0
ClinVar
Risk rs587783459(A;A)
Alt rs587783459(A;A)
Reference rs587783459(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61775190G>A
CLNSRC
CLNACC RCV000145698.1,