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rs121434339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434339(G;G)
Make rs121434339(G;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position60830569
GeneCHD7
is asnp
is mentioned by
dbSNPrs121434339
ebirs121434339
HLIrs121434339
Exacrs121434339
Varsomers121434339
Maprs121434339
PheGenIrs121434339
hapmaprs121434339
1000 genomesrs121434339
hgdprs121434339
ensemblrs121434339
gopubmedrs121434339
geneviewrs121434339
scholarrs121434339
googlers121434339
pharmgkbrs121434339
gwascentralrs121434339
openSNPrs121434339
23andMers121434339
23andMe allrs121434339
SNP Nexus

SNPshotrs121434339
SNPdbers121434339
MSV3drs121434339
GWAS Ctlgrs121434339
Max Magnitude0
OMIM608892
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434339(G;G)
Alt rs121434339(G;G)
Reference rs121434339(T;T)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61743128T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002101.3,