Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10014396
SNCA
1.000 0.040 4 89791478 intron variant T/C snv 0.17 1
rs10079250
CSF1R
0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs1013639215
PITX3
1.000 0.040 10 102231987 missense variant C/G;T snv 4.1E-06 1
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 6
rs10214163
SV2C
1.000 0.040 5 75998585 intergenic variant C/A;T snv 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10247962
TFR2
1.000 0.040 7 100622306 intron variant G/A snv 0.88 2
rs10256359
LOC105375186
1.000 0.040 7 23084258 intergenic variant C/T snv 0.47 1
rs10380
MTRR
0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 6
rs10410544
SIRT2
0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs1043424
PINK1-AS ; PINK1
1.000 0.040 1 20650507 missense variant A/C snv 0.29 0.28 1
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs10445337
MAPT
0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15 3
rs10445338
MAPT
1.000 0.040 17 45990316 intron variant G/A snv 0.15 2
rs10445364
MAPT-AS1
1.000 0.040 17 45838990 intron variant G/A;C snv 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10463554
PAM
1.000 0.040 5 102983270 intron variant T/A;C snv 1
rs1048230
SLC11A2
0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 5
rs1048603
USP40
1.000 0.040 2 233485841 missense variant G/A;T snv 0.32; 1.6E-05 1
rs104893863
QDPR
0.925 0.120 4 17511987 missense variant C/T snv 1.4E-05 2
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21