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rs878855031

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878855031(A;T)
Make rs878855031(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position60822022
GeneCHD7
is asnp
is mentioned by
dbSNPrs878855031
ebirs878855031
HLIrs878855031
Exacrs878855031
Varsomers878855031
Maprs878855031
PheGenIrs878855031
hapmaprs878855031
1000 genomesrs878855031
hgdprs878855031
ensemblrs878855031
gopubmedrs878855031
geneviewrs878855031
scholarrs878855031
googlers878855031
pharmgkbrs878855031
gwascentralrs878855031
openSNPrs878855031
23andMers878855031
23andMe allrs878855031
SNP Nexus

SNPshotrs878855031
SNPdbers878855031
MSV3drs878855031
GWAS Ctlgrs878855031
Max Magnitude0
ClinVar
Risk rs878855031(T;T)
Alt rs878855031(T;T)
Reference rs878855031(A;A)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61734581A>T
CLNSRC
CLNACC RCV000232661.1,