Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518923
PKD1
0.925 0.200 16 2115395 frameshift variant -/C delins 3
rs16347
IL1A
0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70 2
rs777476179
ALMS1
0.851 0.280 2 73448259 frameshift variant A/- del 1.4E-05 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs730947 0.925 0.080 2 218838575 upstream gene variant A/C snv 1.0E-01 2
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs145640112
KLKB1
0.925 0.080 4 186250267 missense variant A/C;G snv 1.8E-04; 4.0E-06 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9