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rs587783445

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783445(G;G)
Make rs587783445(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60850538
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783445
ebirs587783445
HLIrs587783445
Exacrs587783445
Varsomers587783445
Maprs587783445
PheGenIrs587783445
hapmaprs587783445
1000 genomesrs587783445
hgdprs587783445
ensemblrs587783445
gopubmedrs587783445
geneviewrs587783445
scholarrs587783445
googlers587783445
pharmgkbrs587783445
gwascentralrs587783445
openSNPrs587783445
23andMers587783445
23andMe allrs587783445
SNP Nexus

SNPshotrs587783445
SNPdbers587783445
MSV3drs587783445
GWAS Ctlgrs587783445
Max Magnitude0
ClinVar
Risk rs587783445(G;G)
Alt rs587783445(G;G)
Reference rs587783445(T;T)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61763097T>G
CLNSRC
CLNACC RCV000145676.1,