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rs587783434

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783434(G;T)
Make rs587783434(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60821907
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783434
ebirs587783434
HLIrs587783434
Exacrs587783434
Varsomers587783434
Maprs587783434
PheGenIrs587783434
hapmaprs587783434
1000 genomesrs587783434
hgdprs587783434
ensemblrs587783434
gopubmedrs587783434
geneviewrs587783434
scholarrs587783434
googlers587783434
pharmgkbrs587783434
gwascentralrs587783434
openSNPrs587783434
23andMers587783434
23andMe allrs587783434
SNP Nexus

SNPshotrs587783434
SNPdbers587783434
MSV3drs587783434
GWAS Ctlgrs587783434
Max Magnitude0
ClinVar
Risk rs587783434(T;T)
Alt rs587783434(T;T)
Reference rs587783434(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61734466G>T
CLNSRC
CLNACC RCV000145660.1,