Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs5435
SLC2A4
0.851 0.200 17 7283804 missense variant T/A;C snv 0.65 6
rs4606565
DHX37
1.000 0.040 12 124954003 splice region variant A/G snv 0.65 0.57 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 7
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 6
rs12632110
SEMA3F
1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1056534
FN3K ; TBCD
0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
rs1042615
AVPR1A
1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
rs7528153
VAV3
0.925 0.080 1 107765105 missense variant T/A snv 0.58 0.64 4
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs3753886
TAF5L
1.000 0.040 1 229602423 synonymous variant T/A;G snv 5.2E-05; 0.56 2
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs734312
WFS1
0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10
rs2536512
SOD3
0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2047866
UBE2Q2
1.000 0.040 15 75843853 splice region variant C/T snv 0.54 0.43 3
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs7896005
SIRT1
0.925 0.080 10 67891367 intron variant A/G;T snv 0.52; 8.0E-06 0.47 4