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rs121434466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121434466(A;G)
Make rs121434466(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position4269
GeneADAM11
is asnp
is mentioned by
dbSNPrs121434466
ebirs121434466
HLIrs121434466
Exacrs121434466
Varsomers121434466
Maprs121434466
PheGenIrs121434466
hapmaprs121434466
1000 genomesrs121434466
hgdprs121434466
ensemblrs121434466
gopubmedrs121434466
geneviewrs121434466
scholarrs121434466
googlers121434466
pharmgkbrs121434466
gwascentralrs121434466
openSNPrs121434466
23andMers121434466
23andMe allrs121434466
SNP Nexus

SNPshotrs121434466
SNPdbers121434466
MSV3drs121434466
GWAS Ctlgrs121434466
Max Magnitude0
ClinVar
Risk rs121434466(G;G)
Alt rs121434466(G;G)
Reference rs121434466(A;A)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene
CLNDBN Cardiomyopathy, fatal
Reversed 0
HGVS NC_012920.1:m.4269A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010225.4,