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rs587783446

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783446(C;T)
Make rs587783446(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60850546
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783446
ebirs587783446
HLIrs587783446
Exacrs587783446
Varsomers587783446
Maprs587783446
PheGenIrs587783446
hapmaprs587783446
1000 genomesrs587783446
hgdprs587783446
ensemblrs587783446
gopubmedrs587783446
geneviewrs587783446
scholarrs587783446
googlers587783446
pharmgkbrs587783446
gwascentralrs587783446
openSNPrs587783446
23andMers587783446
23andMe allrs587783446
SNP Nexus

SNPshotrs587783446
SNPdbers587783446
MSV3drs587783446
GWAS Ctlgrs587783446
Max Magnitude0
ClinVar
Risk rs587783446(T;T)
Alt rs587783446(T;T)
Reference rs587783446(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61763105C>T
CLNSRC
CLNACC RCV000145677.1,