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rs121434471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434471(C;C)
Make rs121434471(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position4291
GeneADAM11
is asnp
is mentioned by
dbSNPrs121434471
ebirs121434471
HLIrs121434471
Exacrs121434471
Varsomers121434471
Maprs121434471
PheGenIrs121434471
hapmaprs121434471
1000 genomesrs121434471
hgdprs121434471
ensemblrs121434471
gopubmedrs121434471
geneviewrs121434471
scholarrs121434471
googlers121434471
pharmgkbrs121434471
gwascentralrs121434471
openSNPrs121434471
23andMers121434471
23andMe allrs121434471
SNP Nexus

SNPshotrs121434471
SNPdbers121434471
MSV3drs121434471
GWAS Ctlgrs121434471
Max Magnitude0
ClinVar
Risk rs121434471(C;C)
Alt rs121434471(C;C)
Reference rs121434471(T;T)
Significance Pathogenic
Disease Hypertension
Variation info
Gene
CLNDBN Hypertension, hypercholesterolemia, and hypomagnesemia, mitochondrial
Reversed 0
HGVS NC_012920.1:m.4291T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010230.2,