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

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_014321.4(ORC6):c.-47G>A	rs144065502	0.00280
NM_198578.4(LRRK2):c.5510-9A>G	rs41286460	0.00252
NM_000345.4(SNCA):c.*2320A>T	rs529553259	0.00154
NM_000345.4(SNCA):c.*860T>A	rs577490090	0.00153
NM_001146055.2(SNCA):c.-26+1042G>A	rs372025454	0.00073
NM_000345.4(SNCA):c.*2106G>A	rs555697933	0.00030
NM_000345.4(SNCA):c.-26+15C>T	rs545809130	0.00024
NM_000345.4(SNCA):c.*2291C>T	rs550895688	0.00017
NM_000345.4(SNCA):c.*2277A>C	rs375815714	0.00003
NM_000345.4(SNCA):c.*116C>T	rs144511886
NM_000345.4(SNCA):c.*2227C>A	rs551886776
NM_000345.4(SNCA):c.*77C>A	rs145304567
NM_000345.4(SNCA):c.249G>A (p.Glu83=)	rs1737224483
NM_004181.5(UCHL1):c.326-4del	rs3214812
NM_018206.6(VPS35):c.*762dup	rs34926621

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