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rs121434342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434342(G;T)
Make rs121434342(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position60836105
GeneCHD7
is asnp
is mentioned by
dbSNPrs121434342
ebirs121434342
HLIrs121434342
Exacrs121434342
Varsomers121434342
Maprs121434342
PheGenIrs121434342
hapmaprs121434342
1000 genomesrs121434342
hgdprs121434342
ensemblrs121434342
gopubmedrs121434342
geneviewrs121434342
scholarrs121434342
googlers121434342
pharmgkbrs121434342
gwascentralrs121434342
openSNPrs121434342
23andMers121434342
23andMe allrs121434342
SNP Nexus

SNPshotrs121434342
SNPdbers121434342
MSV3drs121434342
GWAS Ctlgrs121434342
Max Magnitude0
OMIM608892
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121434342(T;T)
Alt rs121434342(T;T)
Reference rs121434342(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61748664G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002106.2,