Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10952362 1.000 0.120 7 152565713 regulatory region variant T/C snv 0.25 1
rs11886047 1.000 0.120 2 43623451 upstream gene variant T/A;C snv 0.20 1
rs1249910 1.000 0.120 3 112672327 intergenic variant A/G snv 0.58 1
rs12523822 1.000 0.120 6 154633286 intergenic variant C/G;T snv 1
rs1253192 1.000 0.120 14 59376688 intergenic variant A/G snv 0.92 1
rs16996381 1.000 0.120 22 36115231 intergenic variant G/A snv 0.31 1
rs1866813 1.000 0.120 3 137083096 intergenic variant A/C snv 0.14 1
rs334543 1.000 0.120 3 120113774 intron variant C/A snv 0.74 1
rs1157043147
ACE
1.000 0.120 17 63477150 missense variant T/C snv 2.8E-05 1
rs1341633213
ACE
1.000 0.120 17 63496422 stop gained C/T snv 4.0E-06 1
rs4366
ACE
1.000 0.120 17 63498094 3 prime UTR variant CT/-;CTCT delins 1
rs3807337
CALD1
1.000 0.120 7 134779071 intron variant A/G;T snv 1
rs39075
CHN2
1.000 0.120 7 29237076 intron variant G/A snv 0.41 1
rs2346061
CNDP1
1.000 0.120 18 74533297 upstream gene variant C/A snv 0.71 1
rs7577
CNDP2
1.000 0.120 18 74521112 3 prime UTR variant T/A;C;G snv 0.21 1
rs1252906
DAAM1
1.000 0.120 14 59192073 intron variant A/C;G snv 1
rs1476046
EDN1
1.000 0.120 6 12292988 intron variant G/A snv 0.22 1
rs10951509
ELMO1
1.000 0.120 7 37173878 intron variant G/A;C snv 1
rs1345365
ELMO1
1.000 0.120 7 37161008 intron variant G/A snv 0.61 1
rs9533481
ENOX1
1.000 0.120 13 43415049 intron variant T/C snv 0.78 1
rs10868025
FRMD3
1.000 0.120 9 83549261 intergenic variant A/G snv 0.30 1
rs838136
FUT1
1.000 0.120 19 48753131 intron variant T/C snv 0.41 1
rs1129456
GREM1
1.000 0.120 15 32734466 3 prime UTR variant A/T snv 0.19 1
rs10019835
GUCY1A1
1.000 0.120 4 155712034 intron variant T/A;C snv 1
rs6499323
IL34
1.000 0.120 16 70590580 intron variant A/G snv 0.23 1