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rs587783433

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783433(G;G)
Make rs587783433(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60820036
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783433
ebirs587783433
HLIrs587783433
Exacrs587783433
Varsomers587783433
Maprs587783433
PheGenIrs587783433
hapmaprs587783433
1000 genomesrs587783433
hgdprs587783433
ensemblrs587783433
gopubmedrs587783433
geneviewrs587783433
scholarrs587783433
googlers587783433
pharmgkbrs587783433
gwascentralrs587783433
openSNPrs587783433
23andMers587783433
23andMe allrs587783433
SNP Nexus

SNPshotrs587783433
SNPdbers587783433
MSV3drs587783433
GWAS Ctlgrs587783433
Max Magnitude0
ClinVar
Risk rs587783433(G;G)
Alt rs587783433(G;G)
Reference rs587783433(T;T)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61732595T>G
CLNSRC
CLNACC RCV000145659.1,