Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777583
rs587777583
VARS2
0.800 GeneticVariation UNIPROT Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. 25058219

2014
dbSNP: rs587777583
rs587777583
VARS2
0.800 GeneticVariation UNIPROT VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies. 24827421

2014
dbSNP: rs587777584
rs587777584
VARS2
0.800 GeneticVariation UNIPROT VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies. 24827421

2014
dbSNP: rs587777584
rs587777584
VARS2
0.800 GeneticVariation UNIPROT Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. 25058219

2014
dbSNP: rs587777585
rs587777585
VARS2
0.800 GeneticVariation UNIPROT Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. 25058219

2014
dbSNP: rs587777585
rs587777585
VARS2
0.800 GeneticVariation UNIPROT VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies. 24827421

2014
dbSNP: rs587777583
rs587777583
VARS2
A 0.800 CausalMutation CLINVAR

dbSNP: rs587777584
rs587777584
VARS2
A 0.800 CausalMutation CLINVAR

dbSNP: rs587777585
rs587777585
VARS2
T 0.800 CausalMutation CLINVAR

dbSNP: rs139515727
rs139515727
VARS2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554268077
rs1554268077
VARS2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs775439829
rs775439829
VARS2
C 0.700 GeneticVariation CLINVAR