Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs3738708
PARP1
0.925 0.080 1 226402338 missense variant G/A;C snv 7.0E-06 3
rs374057152
VEGFA
0.925 0.200 6 43777592 missense variant T/C snv 4.0E-06 1.4E-05 3
rs11888095
R3HDM1 ; MIR128-1
2 135665214 intron variant C/T snv 0.17 1
rs1177306304
RREB1
6 7246729 missense variant T/C snv 1
rs1412919356
RREB1
6 7246731 stop gained C/A;T snv 5.3E-06 1
rs1249472918
TMEM189-UBE2V1 ; TMEM189
20 50143583 missense variant A/G snv 4.0E-06 3.5E-05 1
rs73598395
TMEM189-UBE2V1 ; UBE2V1
20 50082842 missense variant G/A snv 1
rs1377510319
ZNF629 ; RNF40
16 30782004 missense variant G/A;C snv 4.7E-06 1