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rs587783441

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783441(A;G)
Make rs587783441(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60837838
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783441
ebirs587783441
HLIrs587783441
Exacrs587783441
Varsomers587783441
Maprs587783441
PheGenIrs587783441
hapmaprs587783441
1000 genomesrs587783441
hgdprs587783441
ensemblrs587783441
gopubmedrs587783441
geneviewrs587783441
scholarrs587783441
googlers587783441
pharmgkbrs587783441
gwascentralrs587783441
openSNPrs587783441
23andMers587783441
23andMe allrs587783441
SNP Nexus

SNPshotrs587783441
SNPdbers587783441
MSV3drs587783441
GWAS Ctlgrs587783441
Max Magnitude0
ClinVar
Risk rs587783441(G;G)
Alt rs587783441(G;G)
Reference rs587783441(A;A)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61750397A>G
CLNSRC
CLNACC RCV000145670.1,