Variant: rs121908686 

    present in Gene: PLA2G6;BAIAP2L2
    present in Chromosome: 22
    Position on Chromosome: 38112558
    Alleles of this Variant: C/T

rs121908686 in PLA2G6;BAIAP2L2 gene and Infantile Neuroaxonal Dystrophy PMID 26196026 2015 PLA2G6-associated Dystonia-Parkinsonism: Case Report and Literature Review.

PMID 20669327 2010 Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.

PMID 27268037 2016 Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.

PMID 26668131 2016 The patients with INAD had PLA2G6 mutations NM_003560.2: c.[950G>T];[426-1077dup] and c.[1799G>A];[2221C>T] and the patient with dystonia-parkinsonism had PLA2G6 mutations NM_003560.2: c.[609G>A];[2222G>A].

PMID 18570303 2009 Characterization of PLA2G6 as a locus for dystonia-parkinsonism.

rs121908686 in PLA2G6;BAIAP2L2 gene and PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE PMID 23279440 2013 EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's disease.

PMID 18570303 2009 Characterization of PLA2G6 as a locus for dystonia-parkinsonism.