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rs587783429

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783429(C;T)
Make rs587783429(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60742912
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783429
ebirs587783429
HLIrs587783429
Exacrs587783429
Varsomers587783429
Maprs587783429
PheGenIrs587783429
hapmaprs587783429
1000 genomesrs587783429
hgdprs587783429
ensemblrs587783429
gopubmedrs587783429
geneviewrs587783429
scholarrs587783429
googlers587783429
pharmgkbrs587783429
gwascentralrs587783429
openSNPrs587783429
23andMers587783429
23andMe allrs587783429
SNP Nexus

SNPshotrs587783429
SNPdbers587783429
MSV3drs587783429
GWAS Ctlgrs587783429
Max Magnitude0
ClinVar
Risk rs587783429(T;T)
Alt rs587783429(T;T)
Reference rs587783429(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61655471C>T
CLNSRC
CLNACC RCV000145653.1,