Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 2
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 1
rs2596551 1.000 0.040 6 31364462 upstream gene variant A/C snv 0.16 1
rs3734526
SLC17A4 ; SLC17A1
1.000 0.040 6 25779508 3 prime UTR variant A/C snv 6.1E-02 1
rs9283880 1.000 0.040 6 27747464 intergenic variant A/C snv 0.34 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 2
rs2383205
CDKN2B-AS1
0.925 0.080 9 22060936 intron variant A/C;G snv 2
rs12091564 1.000 0.040 1 146039391 upstream gene variant A/C;G snv 1
rs2281027
BTN3A3
1.000 0.040 6 26446477 intron variant A/C;G snv 1
rs879254920
LDLR ; MIR6886
0.882 0.120 19 11113665 missense variant A/C;G snv 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 11
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3