rs185645212, POLG

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dementia
CUI: C0497327
Disease: Dementia
0.010 GeneticVariation BEFREE His two siblings were also homozygous with respect to the p.R722H mutation and presented with dementia and sensorineural hearing impairment. 20438629 2010