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rs587783457

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783457(C;T)
Make rs587783457(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60862256
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783457
ebirs587783457
HLIrs587783457
Exacrs587783457
Varsomers587783457
Maprs587783457
PheGenIrs587783457
hapmaprs587783457
1000 genomesrs587783457
hgdprs587783457
ensemblrs587783457
gopubmedrs587783457
geneviewrs587783457
scholarrs587783457
googlers587783457
pharmgkbrs587783457
gwascentralrs587783457
openSNPrs587783457
23andMers587783457
23andMe allrs587783457
SNP Nexus

SNPshotrs587783457
SNPdbers587783457
MSV3drs587783457
GWAS Ctlgrs587783457
Max Magnitude0
ClinVar
Risk rs587783457(T;T)
Alt rs587783457(T;T)
Reference rs587783457(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61774815C>T
CLNSRC
CLNACC RCV000145696.1,