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rs587783451

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783451(A;G)
Make rs587783451(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60853012
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783451
ebirs587783451
HLIrs587783451
Exacrs587783451
Varsomers587783451
Maprs587783451
PheGenIrs587783451
hapmaprs587783451
1000 genomesrs587783451
hgdprs587783451
ensemblrs587783451
gopubmedrs587783451
geneviewrs587783451
scholarrs587783451
googlers587783451
pharmgkbrs587783451
gwascentralrs587783451
openSNPrs587783451
23andMers587783451
23andMe allrs587783451
SNP Nexus

SNPshotrs587783451
SNPdbers587783451
MSV3drs587783451
GWAS Ctlgrs587783451
Max Magnitude0
ClinVar
Risk rs587783451(G;G)
Alt rs587783451(G;G)
Reference rs587783451(A;A)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61765571A>G
CLNSRC
CLNACC RCV000145684.1,