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rs587783456

From SNPedia

Orientationplus
Geno Mag Summary
(TCTT;TCTT) 0 common in clinvar
Make rs587783456(-;-)
Make rs587783456(-;TCTT)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60856664
GeneCHD7
is asnp
is mentioned by
dbSNPrs587783456
ebirs587783456
HLIrs587783456
Exacrs587783456
Varsomers587783456
Maprs587783456
PheGenIrs587783456
hapmaprs587783456
1000 genomesrs587783456
hgdprs587783456
ensemblrs587783456
gopubmedrs587783456
geneviewrs587783456
scholarrs587783456
googlers587783456
pharmgkbrs587783456
gwascentralrs587783456
openSNPrs587783456
23andMers587783456
23andMe allrs587783456
SNP Nexus

SNPshotrs587783456
SNPdbers587783456
MSV3drs587783456
GWAS Ctlgrs587783456
Max Magnitude0
ClinVar
Risk rs587783456(;)
Alt rs587783456(;)
Reference rs587783456(TCTT;TCTT)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61769223_61769226delTCTT
CLNSRC
CLNACC RCV000145692.1,