Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs80356537
ATP1A3
0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs1245342105
SPTBN1
1.000 0.040 2 54622367 missense variant T/C snv 4.0E-06 2
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs1315695444
SELP
1.000 0.040 1 169611580 missense variant C/G snv 4.0E-06 1.4E-05 2