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rs121434476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434476(C;C)
Make rs121434476(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position10010
GeneOR11M1P
is asnp
is mentioned by
dbSNPrs121434476
ebirs121434476
HLIrs121434476
Exacrs121434476
Varsomers121434476
Maprs121434476
PheGenIrs121434476
hapmaprs121434476
1000 genomesrs121434476
hgdprs121434476
ensemblrs121434476
gopubmedrs121434476
geneviewrs121434476
scholarrs121434476
googlers121434476
pharmgkbrs121434476
gwascentralrs121434476
openSNPrs121434476
23andMers121434476
23andMe allrs121434476
SNP Nexus

SNPshotrs121434476
SNPdbers121434476
MSV3drs121434476
GWAS Ctlgrs121434476
Max Magnitude0
ClinVar
Risk rs121434476(C;C)
Alt rs121434476(C;C)
Reference rs121434476(T;T)
Significance Pathogenic
Disease Exercise intolerance
Variation info
Gene
CLNDBN Exercise intolerance
Reversed 0
HGVS NC_012920.1:m.10010T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010236.4,