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rs587783443

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783443(-;-)
Make rs587783443(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60841744
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783443
ebirs587783443
HLIrs587783443
Exacrs587783443
Varsomers587783443
Maprs587783443
PheGenIrs587783443
hapmaprs587783443
1000 genomesrs587783443
hgdprs587783443
ensemblrs587783443
gopubmedrs587783443
geneviewrs587783443
scholarrs587783443
googlers587783443
pharmgkbrs587783443
gwascentralrs587783443
openSNPrs587783443
23andMers587783443
23andMe allrs587783443
SNP Nexus

SNPshotrs587783443
SNPdbers587783443
MSV3drs587783443
GWAS Ctlgrs587783443
Max Magnitude0
ClinVar
Risk rs587783443(;)
Alt rs587783443(;)
Reference rs587783443(T;T)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61754303delT
CLNSRC
CLNACC RCV000145673.1,