| | | Copy number loss | See cases | |
| | LOC129994229, LOC129994230 +688 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129994389, LOC129994390 +340 more | Copy number loss | See cases | |
| | LOC129389350, LOC129389351 +377 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129994580, LOC129994581 +336 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (5 prime UTR variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (5 prime UTR variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (5 prime UTR variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (5 prime UTR variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (intron variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (intron variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (splice donor variant +1 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (intron variant) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | Parkinson Disease, Dominant/Recessive +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (synonymous variant +2 more) | Parkinson Disease, Dominant/Recessive +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (intron variant) | Parkinson Disease, Dominant/Recessive | |
| | MGC32805, SNCAIP (E67G +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | MGC32805, SNCAIP (V393A +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | MGC32805, SNCAIP (V508I +6 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | MGC32805, SNCAIP (H161R +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | MGC32805, SNCAIP (V79A +6 more) | Single nucleotide variant (missense variant +1 more) | Parkinson Disease, Dominant/Recessive | |
| | MGC32805, SNCAIP (A121T +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | MGC32805, SNCAIP (R131Q +6 more) | Single nucleotide variant (missense variant +1 more) | Parkinson Disease, Dominant/Recessive | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | MGC32805, SNCAIP (K158R +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | MGC32805, SNCAIP (E182K +6 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | MGC32805, SNCAIP (G150D +6 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | MGC32805, SNCAIP (K209T +6 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | MGC32805, SNCAIP (S544C +6 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Parkinson Disease, Dominant/Recessive | |
| | MGC32805, SNCAIP (R653W +6 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | MGC32805, SNCAIP (R202Q +6 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Parkinson Disease, Dominant/Recessive | |