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rs878855032

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855032(C;G)
Make rs878855032(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position60830567
GeneCHD7
is asnp
is mentioned by
dbSNPrs878855032
ebirs878855032
HLIrs878855032
Exacrs878855032
Varsomers878855032
Maprs878855032
PheGenIrs878855032
hapmaprs878855032
1000 genomesrs878855032
hgdprs878855032
ensemblrs878855032
gopubmedrs878855032
geneviewrs878855032
scholarrs878855032
googlers878855032
pharmgkbrs878855032
gwascentralrs878855032
openSNPrs878855032
23andMers878855032
23andMe allrs878855032
SNP Nexus

SNPshotrs878855032
SNPdbers878855032
MSV3drs878855032
GWAS Ctlgrs878855032
Max Magnitude0
ClinVar
Risk rs878855032(G;G)
Alt rs878855032(G;G)
Reference rs878855032(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61743126C>G
CLNSRC
CLNACC RCV000234220.1,