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rs587783442

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783442(C;T)
Make rs587783442(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60838202
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783442
ebirs587783442
HLIrs587783442
Exacrs587783442
Varsomers587783442
Maprs587783442
PheGenIrs587783442
hapmaprs587783442
1000 genomesrs587783442
hgdprs587783442
ensemblrs587783442
gopubmedrs587783442
geneviewrs587783442
scholarrs587783442
googlers587783442
pharmgkbrs587783442
gwascentralrs587783442
openSNPrs587783442
23andMers587783442
23andMe allrs587783442
SNP Nexus

SNPshotrs587783442
SNPdbers587783442
MSV3drs587783442
GWAS Ctlgrs587783442
Max Magnitude0
ClinVar
Risk rs587783442(T;T)
Alt rs587783442(T;T)
Reference rs587783442(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61750761C>T
CLNSRC
CLNACC RCV000145671.2,