List of variants reported as benign for Parkinson disease 13, autosomal dominant, susceptibility to

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_181575.5(AUP1):c.129C>G (p.Leu43=)	rs1183739	0.11203
NM_013247.5(HTRA2):c.*94C>T	rs79220020	0.03334
NM_032603.5(LOXL3):c.*237G>T	rs71640295	0.02253
NM_013247.5(HTRA2):c.480C>G (p.Ala160=)	rs2231248	0.01771
NM_013247.5(HTRA2):c.421G>T (p.Ala141Ser)	rs72470544	0.01709
NM_032603.5(LOXL3):c.*90T>C	rs114661282	0.01397
NM_013247.5(HTRA2):c.215T>C (p.Leu72Pro)	rs150047108	0.00200
NM_032603.5(LOXL3):c.*178A>T	rs71640296	0.00039
NM_013247.4(HTRA2):c.-146G>A	rs569404179	0.00001

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