Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs8173
AURKA
0.763 0.240 20 56369735 3 prime UTR variant C/G;T snv 9
rs3024270
H19 ; HOTS ; MRPL23
0.776 0.200 11 1996209 non coding transcript exon variant C/G;T snv 0.46; 5.2E-06 8
rs63750852
PSEN1
0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 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
rs587777074
TUBB4A
0.790 0.240 19 6495688 missense variant C/T snv 4.0E-06 7
rs59912467
STK11
0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 7
rs63751163
PSEN1
0.807 0.120 14 73192844 missense variant T/C snv 7
rs74315355
PINK1 ; PINK1-AS
0.790 0.080 1 20644639 missense variant G/A snv 7
rs761051758
HSPB1
0.827 0.160 7 76302805 synonymous variant G/A snv 8.5E-06 7
rs869312966
SCN8A
0.827 0.120 12 51806345 missense variant G/T snv 7
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs104893856
PHOX2B
0.827 0.080 4 41746162 missense variant C/T snv 6
rs104894103
APTX
0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs121908513
SPAST
0.807 0.280 2 32116145 missense variant T/A snv 6
rs121912452
SOD1
0.807 0.120 21 31667271 missense variant T/C;G snv 4.0E-06 6
rs1285675735
SORD
0.827 0.200 15 45043384 synonymous variant C/G;T snv 1.1E-05; 1.1E-05 6
rs4500567
TSPAN8
0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs4884357
TARDBP
0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 6
rs538874513
TP73
0.807 0.120 1 3730017 missense variant C/G;T snv 8.2E-06; 8.2E-06 6
rs63749805
PSEN1
0.807 0.120 14 73173577 missense variant C/G;T snv 6