ClinVar Miner

List of variants in gene VPS35 reported as benign for Parkinson disease

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_018206.6(VPS35):c.1938C>T (p.His646=) rs168745 0.97484
NM_018206.6(VPS35):c.1938= (p.His646=) rs168745 0.02516
NM_018206.6(VPS35):c.1145A>G (p.Lys382Arg) rs116254156 0.00480
NM_018206.6(VPS35):c.1398G>A (p.Thr466=) rs150810185 0.00274
NM_018206.6(VPS35):c.2241C>T (p.Ile747=) rs140543776 0.00159
NM_018206.6(VPS35):c.834T>C (p.Thr278=) rs148572750 0.00093
NM_018206.6(VPS35):c.*422C>A rs181198454 0.00079
NM_018206.6(VPS35):c.2145A>G (p.Leu715=) rs145033509 0.00052
NM_018206.6(VPS35):c.*346G>A rs545755034 0.00029
NM_018206.6(VPS35):c.151G>A (p.Gly51Ser) rs193077277 0.00028
NM_018206.6(VPS35):c.1268C>T (p.Pro423Leu) rs373075116 0.00012
NM_018206.6(VPS35):c.1420C>G (p.Gln474Glu) rs370401767 0.00006
NM_018206.6(VPS35):c.*354G>C rs572048744 0.00001
NM_018206.6(VPS35):c.2122A>C (p.Asn708His) rs199940967 0.00001
NM_018206.6(VPS35):c.1368+15A>G
NM_018206.6(VPS35):c.199+8T>C
NM_018206.6(VPS35):c.915-16T>G rs757051230
NM_018206.6(VPS35):c.915-3del rs569369937

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