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rs587783436

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587783436(-;-)
Make rs587783436(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60822093
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783436
ebirs587783436
HLIrs587783436
Exacrs587783436
Varsomers587783436
Maprs587783436
PheGenIrs587783436
hapmaprs587783436
1000 genomesrs587783436
hgdprs587783436
ensemblrs587783436
gopubmedrs587783436
geneviewrs587783436
scholarrs587783436
googlers587783436
pharmgkbrs587783436
gwascentralrs587783436
openSNPrs587783436
23andMers587783436
23andMe allrs587783436
SNP Nexus

SNPshotrs587783436
SNPdbers587783436
MSV3drs587783436
GWAS Ctlgrs587783436
Max Magnitude0
ClinVar
Risk rs587783436(;)
Alt rs587783436(;)
Reference rs587783436(AG;AG)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61734652_61734653delAG
CLNSRC
CLNACC RCV000145662.1,