ClinVar Miner

List of variants in gene PLA2G6 reported as uncertain significance for Autosomal recessive Parkinson disease 14

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003560.4(PLA2G6):c.2417C>G (p.Pro806Arg)	rs140758033	0.00021
NM_003560.4(PLA2G6):c.29C>A (p.Thr10Asn)	rs1323819447

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