Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs9526984
KL
1.000 0.040 13 33035800 intron variant A/G snv 5.5E-02 2
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs886039469
KCNMA1-AS1 ; KCNMA1
0.701 0.560 10 76891709 missense variant T/C snv 35
rs876660634
PTEN
0.807 0.200 10 87925551 missense variant A/C;G snv 10
rs863225300
SFTA3 ; NKX2-1 ; NKX2-1-AS1
0.925 0.280 14 36517960 stop gained G/T snv 2
rs863225264
MTOR
0.827 0.240 1 11130747 missense variant C/T snv 6
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs8191664
NEIL2
0.807 0.200 8 11786044 missense variant G/A;C;T snv 4.0E-05; 3.8E-02 7
rs8179176
ESR1
1.000 0.040 6 151842199 intron variant C/A;T snv 1
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs8059356 0.925 0.080 16 86323639 intergenic variant G/A snv 0.32 2
rs80358259
NPC1
0.851 0.320 18 23536736 missense variant A/G snv 2.0E-04 2.4E-04 9
rs80358257
NPC1
0.827 0.280 18 23538564 missense variant G/C snv 1.2E-04 2.1E-04 8
rs80356773
GBA
0.925 0.080 1 155235002 missense variant C/T snv 3
rs80356734
TARDBP
0.851 0.160 1 11022464 missense variant A/G snv 4
rs80356733
TARDBP
0.790 0.200 1 11022451 missense variant G/T snv 7
rs80356537
ATP1A3
0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs80338903
USH2A
0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs80017116 1.000 0.040 3 150064125 intron variant G/A snv 5.6E-03 1
rs799979
CD36
1.000 0.040 7 80415882 intron variant A/G snv 2.7E-02 1
rs79947075 1.000 0.040 17 40764791 downstream gene variant C/T snv 9.5E-03 1