Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35850753
TP53
0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 8
rs774005786
PARK7
0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs28938172
PARK7
0.790 0.080 1 7984981 missense variant T/C snv 7
rs34995376
LRRK2
0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs74315355
PINK1 ; PINK1-AS
0.790 0.080 1 20644639 missense variant G/A snv 7
rs104893856
PHOX2B
0.827 0.080 4 41746162 missense variant C/T snv 6
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs74315351
PARK7
0.807 0.080 1 7962863 missense variant G/A snv 6
rs74315352
PARK7
0.807 0.080 1 7984930 missense variant A/C snv 1.4E-04 5.9E-04 6
rs1438259227
PRKN
0.827 0.080 6 162443428 missense variant T/A snv 7.0E-06 5
rs201216664
NME1-NME2 ; NME2
0.851 0.080 17 51171503 missense variant A/G snv 5
rs2271338
ADGRL3
0.827 0.080 4 61996533 intron variant G/A snv 0.26 5
rs748343847
MIR6084 ; PINK1
0.827 0.080 1 20633708 missense variant G/A snv 6.9E-05 5
rs863225285
ALK
0.851 0.080 2 29209789 missense variant T/G snv 5
rs11037575
HSD17B12
0.882 0.080 11 43706780 intron variant T/C snv 0.36 4
rs11103603 0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46 4
rs11669203
MAP2K7 ; TGFBR3L
0.882 0.080 19 7914916 upstream gene variant G/C snv 0.15 4
rs121908531
YARS2 ; DNM1L
0.851 0.080 12 32731118 missense variant C/A;G snv 4
rs17016074
SNCA
0.851 0.080 4 89726127 3 prime UTR variant G/A snv 4.7E-02 4
rs201668878
UBE4A
0.882 0.080 11 118373576 missense variant T/C snv 1.7E-04 1.0E-04 4
rs221634
LIN28B
0.851 0.080 6 105080213 3 prime UTR variant T/A snv 0.52 4
rs2273267
NRAS ; CSDE1
0.882 0.080 1 114716848 upstream gene variant A/C;T snv 4
rs3768716
BARD1
0.851 0.080 2 214771070 intron variant T/C snv 0.16 4
rs377522479
ARHGAP24
0.882 0.080 4 85931021 missense variant C/T snv 2.0E-05 3.5E-05 4
rs41274458
KIF1B
0.851 0.080 1 10303606 missense variant G/T snv 1.8E-02 1.9E-02 4