Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783448

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783448(A;C)
Make rs587783448(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60852017
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783448
ebirs587783448
HLIrs587783448
Exacrs587783448
Varsomers587783448
Maprs587783448
PheGenIrs587783448
hapmaprs587783448
1000 genomesrs587783448
hgdprs587783448
ensemblrs587783448
gopubmedrs587783448
geneviewrs587783448
scholarrs587783448
googlers587783448
pharmgkbrs587783448
gwascentralrs587783448
openSNPrs587783448
23andMers587783448
23andMe allrs587783448
SNP Nexus

SNPshotrs587783448
SNPdbers587783448
MSV3drs587783448
GWAS Ctlgrs587783448
Max Magnitude0
ClinVar
Risk rs587783448(C;C)
Alt rs587783448(C;C)
Reference rs587783448(A;A)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61764576A>C
CLNSRC
CLNACC RCV000145679.1,