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rs587783432

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783432(A;A)
Make rs587783432(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60816502
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783432
ebirs587783432
HLIrs587783432
Exacrs587783432
Varsomers587783432
Maprs587783432
PheGenIrs587783432
hapmaprs587783432
1000 genomesrs587783432
hgdprs587783432
ensemblrs587783432
gopubmedrs587783432
geneviewrs587783432
scholarrs587783432
googlers587783432
pharmgkbrs587783432
gwascentralrs587783432
openSNPrs587783432
23andMers587783432
23andMe allrs587783432
SNP Nexus

SNPshotrs587783432
SNPdbers587783432
MSV3drs587783432
GWAS Ctlgrs587783432
Max Magnitude0
ClinVar
Risk rs587783432(A;A)
Alt rs587783432(A;A)
Reference rs587783432(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61729061G>A
CLNSRC
CLNACC RCV000145658.1,