List of variants reported as likely benign for Parkinson Disease, Recessive

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_032409.3(PINK1):c.*265G>T	rs512550	0.56246
NM_005216.5(DDOST):c.*462A>G	rs559542	0.43468
NM_032409.3(PINK1):c.*672T>C	rs2078073	0.27437
NM_032409.3(PINK1):c.*564T>G	rs1043502	0.27404
NM_032409.3(PINK1):c.1562A>C (p.Asn521Thr)	rs1043424	0.27338
NM_032409.3(PINK1):c.*196T>C	rs1043443	0.27336
NM_007262.4(PARK7):c.-137G>A	rs17523802	0.22239
NM_032409.3(PINK1):c.*415C>G	rs8064	0.14517
NM_005216.5(DDOST):c.*457A>C	rs150466875	0.05391
NM_007262.5(PARK7):c.234C>T (p.Gly78=)	rs11548937	0.03501
NM_005216.5(DDOST):c.831C>T (p.Ala277=)	rs6692016	0.02273
NM_032409.3(PINK1):c.*490A>C	rs16824318	0.02268
NM_005216.5(DDOST):c.375_376dup	rs200971370
NM_005216.5(DDOST):c.*542TAAA[6]	rs78039244
NM_032409.3(PINK1):c.573_576dup	rs143763511
NM_032409.3(PINK1):c.673_675dup	rs3077908
NM_032409.3(PINK1):c.*725GA[4]	rs34361349

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