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rs587783428

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783428(G;T)
Make rs587783428(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60742678
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783428
ebirs587783428
HLIrs587783428
Exacrs587783428
Varsomers587783428
Maprs587783428
PheGenIrs587783428
hapmaprs587783428
1000 genomesrs587783428
hgdprs587783428
ensemblrs587783428
gopubmedrs587783428
geneviewrs587783428
scholarrs587783428
googlers587783428
pharmgkbrs587783428
gwascentralrs587783428
openSNPrs587783428
23andMers587783428
23andMe allrs587783428
SNP Nexus

SNPshotrs587783428
SNPdbers587783428
MSV3drs587783428
GWAS Ctlgrs587783428
Max Magnitude0
ClinVar
Risk rs587783428(T;T)
Alt rs587783428(T;T)
Reference rs587783428(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61655237G>T
CLNSRC
CLNACC RCV000145652.1,