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rs587783455

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783455(C;T)
Make rs587783455(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60856532
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783455
ebirs587783455
HLIrs587783455
Exacrs587783455
Varsomers587783455
Maprs587783455
PheGenIrs587783455
hapmaprs587783455
1000 genomesrs587783455
hgdprs587783455
ensemblrs587783455
gopubmedrs587783455
geneviewrs587783455
scholarrs587783455
googlers587783455
pharmgkbrs587783455
gwascentralrs587783455
openSNPrs587783455
23andMers587783455
23andMe allrs587783455
SNP Nexus

SNPshotrs587783455
SNPdbers587783455
MSV3drs587783455
GWAS Ctlgrs587783455
Max Magnitude0
ClinVar
Risk rs587783455(T;T)
Alt rs587783455(T;T)
Reference rs587783455(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61769091C>T
CLNSRC
CLNACC RCV000145690.1,