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rs587783440

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783440(C;T)
Make rs587783440(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60837800
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783440
ebirs587783440
HLIrs587783440
Exacrs587783440
Varsomers587783440
Maprs587783440
PheGenIrs587783440
hapmaprs587783440
1000 genomesrs587783440
hgdprs587783440
ensemblrs587783440
gopubmedrs587783440
geneviewrs587783440
scholarrs587783440
googlers587783440
pharmgkbrs587783440
gwascentralrs587783440
openSNPrs587783440
23andMers587783440
23andMe allrs587783440
SNP Nexus

SNPshotrs587783440
SNPdbers587783440
MSV3drs587783440
GWAS Ctlgrs587783440
Max Magnitude0
ClinVar
Risk rs587783440(T;T)
Alt rs587783440(T;T)
Reference rs587783440(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61750359C>T
CLNSRC
CLNACC RCV000145669.1,