Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11616662 13 40545329 intron variant G/A snv 0.11 2
rs11790360
LINC02692
9 136971795 non coding transcript exon variant T/C;G snv 1.5E-05; 0.49 2
rs12448211 16 88296907 intron variant G/A snv 0.56 2
rs12913547
SMAD3
15 67175169 intron variant T/C;G snv 2
rs2755237
LINC00598
13 40535292 intron variant A/C snv 0.17 2
rs3118520 9 134549749 upstream gene variant A/G snv 0.49 2
rs4792535 17 14661813 intergenic variant C/T snv 0.45 2
rs4938174 11 111042516 upstream gene variant G/A snv 0.31 2
rs6540223 16 88287830 intron variant C/T snv 0.72 2
rs7040970 9 136964561 upstream gene variant T/C snv 0.44 2
rs752092
CHSY1
15 101241729 intron variant A/G snv 0.43 2
rs785422
TJP1
15 29881682 intron variant C/T snv 1.0E-01 2
rs930847
LRRK1
15 101018357 intron variant G/T snv 0.67 2
rs96067
COL8A2
1 36106319 intron variant G/A snv 0.73 2
rs9822953
LINC00886
3 156754282 intron variant C/G;T snv 2
rs1007000
LPAR1
9 110900401 intron variant C/T snv 0.16 1
rs10163187
ADAMTS7P4
15 85327287 intron variant C/T snv 0.29 1
rs10189064
USP37
2 218462777 intron variant G/A snv 2.1E-02 1
rs1034200 13 22654552 intergenic variant C/A;T snv 1
rs10434530
LOC107986419
5 65080521 intergenic variant T/A;C snv 1
rs10520600
LOC102724393
15 85365171 intergenic variant A/G snv 0.15 1
rs10842183
SOX5
12 23580508 intron variant G/A snv 0.78 1
rs11145951 9 136965812 upstream gene variant T/C snv 0.44 1
rs1117707
LOC107986419
5 65093838 intergenic variant A/G;T snv 1
rs11204213
RBP3
10 47351134 missense variant G/A snv 6.8E-03 2.7E-03 1