Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs113994097
POLG
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs41549716
POLG
0.882 0.200 15 89321842 missense variant T/C snv 6.6E-03 7.0E-03 4
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs774005786
PARK7
0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs71653619
PARK7
1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs1417802320
PARK7
1 7962861 missense variant A/T snv 4.0E-06 1
rs137852538
PGK1
0.925 0.080 X 78117385 missense variant A/T snv 3
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 4
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs63750802
PSEN1
0.851 0.080 14 73219144 missense variant T/G snv 7
rs63750050
PSEN1
0.925 0.080 14 73198106 missense variant T/G snv 5
rs63750680
PSEN1
1.000 0.080 14 73198076 missense variant T/C snv 2
rs63750444
PSEN1
0.882 0.080 14 73192745 missense variant G/A snv 4
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs63750522
PSEN1
0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs1555507479
GNAO1
0.807 0.160 16 56336799 missense variant C/A snv 12
rs1290141855
SLC6A2
1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3