List of variants in gene combination PACRG, PRKN reported as uncertain significance for autosomal recessive juvenile Parkinson disease 2

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004562.3(PRKN):c.-42T>C	rs112850281	0.00042
NM_004562.3(PRKN):c.-46C>T	rs369389244	0.00011
NM_004562.3(PRKN):c.-85G>A	rs556535340	0.00004
NM_004562.3(PRKN):c.-57G>C	rs750626864	0.00001
NM_004562.3(PRKN):c.-78C>A	rs765761156
NM_004562.3(PRKN):c.7+4C>T	rs749081702

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