Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11377084
LINC01169
15 66651883 intron variant -/A ins 0.67 1
rs111476047 19 49548304 downstream gene variant -/GGTT delins 0.37 1
rs2858942
HBA1
16 175654 upstream gene variant A/C snv 0.76 2
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs2878889
SMAD7
18 48936766 intron variant A/C;G;T snv 2
rs146109634
BTNL2 ; TSBP1-AS1
6 32400784 intron variant A/C;G;T snv 1
rs11089824 22 37113146 upstream gene variant A/C;T snv 4
rs7560180
PSD4
2 113207623 3 prime UTR variant A/C;T snv 1
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs11072566
NRG4
0.925 0.120 15 76001630 intron variant A/G snv 0.45 5
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs9310736
THRB
3 24309320 intron variant A/G snv 0.69 4
rs17563683
LOC107985028 ; LINC02210-CRHR1
17 45733706 intron variant A/G snv 0.15 3
rs17773190
LINC01118
2 46803224 intron variant A/G snv 0.32 3