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rs863224856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224856(-;T)
Make rs863224856(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60845398
GeneCHD7
is asnp
is mentioned by
dbSNPrs863224856
ClinGenrs863224856
ebirs863224856
HLIrs863224856
Exacrs863224856
Varsomers863224856
Maprs863224856
PheGenIrs863224856
hapmaprs863224856
1000 genomesrs863224856
hgdprs863224856
ensemblrs863224856
gopubmedrs863224856
geneviewrs863224856
scholarrs863224856
googlers863224856
pharmgkbrs863224856
gwascentralrs863224856
openSNPrs863224856
23andMers863224856
23andMe allrs863224856
SNP Nexus

SNPshotrs863224856
SNPdbers863224856
MSV3drs863224856
GWAS Ctlgrs863224856
Max Magnitude0
ClinVar
Risk rs863224856(T;T)
Alt rs863224856(T;T)
Reference Rs863224856(-;-)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61757957dupT
CLNSRC
CLNACC RCV000198147.1,