Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs897984
MIR762HG ; BCL7C ; MIR4519
0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs377591051
PRKN
0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs1446915570
PSEN1
0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs777296100
SNCA
0.925 0.080 4 89725318 3 prime UTR variant -/TAA;TAAAA ins 2
rs1342971994
SNCA
1.000 0.080 4 89822344 missense variant C/T snv 1.4E-05 1
rs7681440
SNCA-AS1 ; SNCA
1.000 0.080 4 89835399 intron variant C/A;G snv 1
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs1330229174
SNCA ; SNCA-AS1
0.925 0.080 4 89835568 missense variant T/C snv 4.0E-06 2
rs104893936
SNCB
0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs104893937
SNCB
0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5