Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs7660895
SLC2A9
0.882 0.200 4 9983821 intron variant A/G;T snv 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv 4
rs10821905
A1CF
0.925 0.120 10 50886333 upstream gene variant G/A;T snv 4
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs11554266
GNAS
1.000 0.040 20 58903791 splice region variant C/G;T snv 4.0E-06; 2.3E-03 4
rs1165151
SLC17A1
0.925 0.120 6 25821388 intron variant T/A;G snv 4
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 4
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1165205
SLC17A3
0.925 0.120 6 25870314 intron variant T/A;G snv 4
rs1184804
SLC17A3
0.925 0.120 6 25867998 intron variant T/A;C snv 4
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4
rs147445322
KCNQ1-AS1 ; KCNQ1
0.882 0.120 11 2847803 missense variant G/A;T snv 7.2E-05; 5.5E-06 4
rs150551
CARMIL1
0.925 0.120 6 25533702 intron variant A/G;T snv 4
rs1540275 0.925 0.120 6 26036248 upstream gene variant T/A;C snv 4
rs201874364
ETV5
1.000 0.040 3 186065822 missense variant C/A;T snv 4.0E-06; 7.2E-05 4
rs202007714
SLC25A26 ; LRIG1
1.000 0.040 3 66383098 missense variant G/A;C snv 1.4E-04; 4.0E-06 4
rs3775948
LOC105374476 ; SLC2A9
0.882 0.160 4 9993558 intron variant G/A;C snv 4
rs4073582
CNIH2
0.925 0.120 11 66283241 splice region variant G/A;C snv 0.27 4
rs6903765
CARMIL1
0.925 0.120 6 25609510 intron variant A/G;T snv 4
rs6905614
SLC17A3
0.925 0.120 6 25840257 intron variant C/A;G snv 4
rs7193778 0.882 0.120 16 69529987 intergenic variant C/G;T snv 4