Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs76151636
ATP7B
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs778361520
ADGRB2
0.925 0.120 1 31728621 missense variant G/A snv 8.0E-06 2.1E-05 9
rs137852642
NOTCH3
0.827 0.200 19 15192242 missense variant G/A;T snv 4.5E-06; 4.5E-06 9
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs118192200
KCNQ2
0.882 20 63444729 missense variant C/T snv 4
rs137853054
PRKN
0.882 0.160 6 161973317 missense variant G/A;C;T snv 3.7E-04; 4.0E-06; 8.0E-06 4
rs571825723
PSEN1
0.925 0.080 14 73211867 missense variant C/T snv 4.4E-05 2.8E-05 4
rs1341026713
APP
0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 3
rs1801582
PRKN
0.925 0.120 6 161386823 missense variant C/G;T snv 0.16; 3.2E-05 3
rs751037529
PRKN
0.925 0.040 6 161785793 missense variant C/G snv 1.2E-05 3
rs797045360
ATP7A ; PGK1
1.000 0.160 X 78015810 missense variant C/T snv 2
rs748860341
GFAP
1.000 0.120 17 44910143 missense variant C/G;T snv 8.0E-06; 8.0E-06 2