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rs587783458

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783458(C;T)
Make rs587783458(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60862322
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783458
ebirs587783458
HLIrs587783458
Exacrs587783458
Varsomers587783458
Maprs587783458
PheGenIrs587783458
hapmaprs587783458
1000 genomesrs587783458
hgdprs587783458
ensemblrs587783458
gopubmedrs587783458
geneviewrs587783458
scholarrs587783458
googlers587783458
pharmgkbrs587783458
gwascentralrs587783458
openSNPrs587783458
23andMers587783458
23andMe allrs587783458
SNP Nexus

SNPshotrs587783458
SNPdbers587783458
MSV3drs587783458
GWAS Ctlgrs587783458
Max Magnitude0
ClinVar
Risk rs587783458(T;T)
Alt rs587783458(T;T)
Reference rs587783458(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61774881C>T
CLNSRC
CLNACC RCV000145697.1,