Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs568700395 17 28753031 upstream gene variant -/A;AA delins 1
rs58565441 17 28753031 upstream gene variant -/A;AA delins 2.1E-05 1
rs200351105
C18orf25
18 46262655 intron variant -/AA delins 1
rs531114901
ATR
3 142496336 intron variant -/ATATCT;ATCT;ATGTATATATATATACATGTATATATATATGTATATATATATATCT;CT delins 9.6E-04 1
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs36075013 3 142281368 regulatory region variant -/G delins 1
rs3215645
SPTB
14 64796872 intron variant -/T delins 0.44 1
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs201794926
PPP1R16A
8 144485527 intron variant A/-;AA;AAA;AAAA delins 2
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs4953318
PRKCE
2 46127912 intron variant A/C snv 0.43 5
rs3804105
CARMIL1
0.925 0.120 6 25612455 intron variant A/C snv 0.29 4
rs9357371
MED20
6 41917581 5 prime UTR variant A/C snv 0.20 4
rs9358903 0.925 0.120 6 26061721 intergenic variant A/C snv 0.38 4
rs9467636
SLC17A2
0.925 0.120 6 25919321 intron variant A/C snv 0.34 4
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 3
rs12201186 0.925 0.120 6 25625367 downstream gene variant A/C snv 0.28 3
rs2871960
ZBTB38
3 141402972 5 prime UTR variant A/C snv 0.55 3
rs10457631 6 135124041 intergenic variant A/C snv 0.25 2
rs11066028
ALDH2
1.000 0.080 12 111807366 intron variant A/C snv 0.45 2