Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1002630
CHN2
0.925 0.160 7 29388454 intron variant G/A snv 0.16 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1043045
SLMAP
1.000 0.120 3 57928451 3 prime UTR variant T/C snv 0.31 1
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs10490924
ARMS2 ; LOC105378525
0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs10491034
ARHGAP22
1.000 0.120 10 48602322 intron variant G/A;T snv 1
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10507875
OBI1-AS1 ; EDNRB
0.925 0.160 13 77943119 intron variant A/G snv 0.17 3
rs1057719
SLMAP
1.000 0.120 3 57927987 3 prime UTR variant A/G snv 0.31 1
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs11018670 0.925 0.160 11 89623460 intergenic variant A/G snv 0.30 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs1136287
SERPINF1
0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs1145612 1.000 0.120 5 158271107 upstream gene variant C/A snv 0.49 1
rs114790220 1.000 0.120 8 5306434 intergenic variant T/A;C snv 1
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11567245
CACNA2D1
1.000 0.120 7 82151406 intron variant T/A snv 1
rs11662496 1.000 0.120 18 43695432 intergenic variant A/G;T snv 1
rs11771617 1.000 0.120 7 125733372 intergenic variant A/G snv 0.20 1