ClinVar Miner

List of variants studied for Autosomal recessive Parkinson disease 14

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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_003560.4(PLA2G6):c.956C>T (p.Thr319Met) rs149653983 0.00029
NM_003560.4(PLA2G6):c.2417C>G (p.Pro806Arg) rs140758033 0.00021
NM_003560.4(PLA2G6):c.2222G>A (p.Arg741Gln) rs121908686 0.00009
NM_003560.4(PLA2G6):c.2239C>T (p.Arg747Trp) rs121908687 0.00003
NM_003560.4(PLA2G6):c.1061T>C (p.Leu354Pro) rs1403125636 0.00001
NM_003560.4(PLA2G6):c.1354C>T (p.Gln452Ter) rs387906864
NM_003560.4(PLA2G6):c.1634A>C (p.Lys545Thr) rs121908681
NM_003560.4(PLA2G6):c.1904G>A (p.Arg635Gln) rs387906863
NM_003560.4(PLA2G6):c.216C>A (p.Phe72Leu) rs774631197
NM_003560.4(PLA2G6):c.29C>A (p.Thr10Asn) rs1323819447
NM_003560.4(PLA2G6):c.797G>C (p.Gly266Ala) rs764286950
NM_003560.4(PLA2G6):c.991G>T (p.Asp331Tyr) rs199935023

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