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rs281865491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865491(C;T)
Make rs281865491(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position66531382
GeneTK2
is asnp
is mentioned by
dbSNPrs281865491
ebirs281865491
HLIrs281865491
Exacrs281865491
Varsomers281865491
Maprs281865491
PheGenIrs281865491
hapmaprs281865491
1000 genomesrs281865491
hgdprs281865491
ensemblrs281865491
gopubmedrs281865491
geneviewrs281865491
scholarrs281865491
googlers281865491
pharmgkbrs281865491
gwascentralrs281865491
openSNPrs281865491
23andMers281865491
23andMe allrs281865491
SNP Nexus

SNPshotrs281865491
SNPdbers281865491
MSV3drs281865491
GWAS Ctlgrs281865491
Max Magnitude0
ClinVar
Risk rs281865491(T;T)
Alt rs281865491(T;T)
Reference rs281865491(C;C)
Significance Pathogenic
Disease Mitochondrial DNA depletion syndrome 2
Variation info
Gene TK2
CLNDBN Mitochondrial DNA depletion syndrome 2
Reversed 1
HGVS NC_000016.9:g.66565285G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032246.1,