Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141773786
NEMP1
12 57081818 intron variant A/C;G snv 0.13 1
rs17817628
LOC107985002 ; STXBP4
17 55097366 intron variant A/C;G snv 1
rs2063730
GAB2
11 78337478 intron variant A/C;G snv 1
rs7115813
JHY
11 122961366 3 prime UTR variant A/C;G snv 1
rs7995668
KLF12
13 74131042 intergenic variant A/C;G snv 1
rs939317
EIF4G1
3 184328011 intron variant A/C;G snv 0.76 0.80 1
rs9616551 22 49284503 intergenic variant A/C;G snv 1
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs11893331
CCDC85A
2 56350271 intron variant A/C;G;T snv 1
rs1915146
CTBP2
10 125157645 intron variant A/C;G;T snv 1
rs2417687
LINC01505
9 106161176 intron variant A/C;G;T snv 1
rs4133019 1 102042537 intergenic variant A/C;G;T snv 1
rs55939240 19 35694201 TF binding site variant A/C;G;T snv 1
rs10895141
TRPC6
11 101566010 intron variant A/C;T snv 0.62 1
rs11071027
UNC13C
15 54072564 intron variant A/C;T snv 1
rs2343506 1 162923134 intergenic variant A/C;T snv 1
rs6438424
LOC107986022
3 117855975 intron variant A/C;T snv 1
rs7135337
HNF1A-AS1
12 120966352 intron variant A/C;T snv 1
rs7643617
ZBTB20
3 115034231 intron variant A/C;T snv 1
rs852033 20 17104848 intergenic variant A/C;T snv 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 4
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs314280
LIN28B
0.925 0.040 6 104952962 intron variant A/G snv 0.46 3