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rs587783447

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783447(G;T)
Make rs587783447(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60851048
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783447
ebirs587783447
HLIrs587783447
Exacrs587783447
Varsomers587783447
Maprs587783447
PheGenIrs587783447
hapmaprs587783447
1000 genomesrs587783447
hgdprs587783447
ensemblrs587783447
gopubmedrs587783447
geneviewrs587783447
scholarrs587783447
googlers587783447
pharmgkbrs587783447
gwascentralrs587783447
openSNPrs587783447
23andMers587783447
23andMe allrs587783447
SNP Nexus

SNPshotrs587783447
SNPdbers587783447
MSV3drs587783447
GWAS Ctlgrs587783447
Max Magnitude0
ClinVar
Risk rs587783447(T;T)
Alt rs587783447(T;T)
Reference rs587783447(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61763607G>T
CLNSRC
CLNACC RCV000145678.1,