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

rs587783431

From SNPedia

Orientationplus
Geno Mag Summary
(CAAA;CAAA) 0 common in clinvar
Make rs587783431(-;-)
Make rs587783431(-;CAAA)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60741623
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783431
ebirs587783431
HLIrs587783431
Exacrs587783431
Varsomers587783431
Maprs587783431
PheGenIrs587783431
hapmaprs587783431
1000 genomesrs587783431
hgdprs587783431
ensemblrs587783431
gopubmedrs587783431
geneviewrs587783431
scholarrs587783431
googlers587783431
pharmgkbrs587783431
gwascentralrs587783431
openSNPrs587783431
23andMers587783431
23andMe allrs587783431
SNP Nexus

SNPshotrs587783431
SNPdbers587783431
MSV3drs587783431
GWAS Ctlgrs587783431
Max Magnitude0
ClinVar
Risk rs587783431(;)
Alt rs587783431(;)
Reference rs587783431(CAAA;CAAA)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61654182_61654185delCAAA
CLNSRC
CLNACC RCV000145655.1,