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rs121434469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434469(C;C)
Make rs121434469(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position4290
GeneADAM11
is asnp
is mentioned by
dbSNPrs121434469
ebirs121434469
HLIrs121434469
Exacrs121434469
Varsomers121434469
Maprs121434469
PheGenIrs121434469
hapmaprs121434469
1000 genomesrs121434469
hgdprs121434469
ensemblrs121434469
gopubmedrs121434469
geneviewrs121434469
scholarrs121434469
googlers121434469
pharmgkbrs121434469
gwascentralrs121434469
openSNPrs121434469
23andMers121434469
23andMe allrs121434469
SNP Nexus

SNPshotrs121434469
SNPdbers121434469
MSV3drs121434469
GWAS Ctlgrs121434469
Max Magnitude0
ClinVar
Risk rs121434469(C;C)
Alt rs121434469(C;C)
Reference rs121434469(T;T)
Significance Pathogenic
Disease Encephalopathy
Variation info
Gene
CLNDBN Encephalopathy, familial progressive necrotizing
Reversed 0
HGVS NC_012920.1:m.4290T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010228.2,