Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7218361 1.000 0.120 17 39569151 downstream gene variant A/G snv 0.97 1
rs846908
HSD11B1-AS1 ; HSD11B1
1.000 0.120 1 209685108 intron variant A/G snv 0.97 1
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs316019
SLC22A2
0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs684846 1.000 0.120 3 183173176 downstream gene variant C/T snv 0.85 1
rs562556
PCSK9
0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs4340576
THADA
1.000 0.120 2 43328367 intron variant T/C snv 0.80 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs363282
PDZD8 ; SLC18A2
1.000 0.120 10 117278157 3 prime UTR variant G/A snv 0.77 1
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs10407022
AMH ; MIR4321
0.882 0.200 19 2249478 missense variant G/T snv 0.77 0.74 3
rs804279 1.000 0.120 8 11766380 upstream gene variant A/T snv 0.72 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs1151996
PPARG
1.000 0.120 3 12404308 intron variant C/A snv 0.70 1
rs1795379
LOC105369844
1.000 0.120 12 75547262 intergenic variant T/C snv 0.70 1
rs10179648
THADA
1.000 0.120 2 43580926 intron variant C/T snv 0.70 1
rs11466313
TGFB1 ; B9D2
1.000 0.120 19 41355432 intron variant -/CTC;CTCATGTCCCTGCCCTCCCTCCTC delins 0.70 1
rs6523
INSL3
0.882 0.200 19 17821329 missense variant T/C snv 0.65 0.70 4
rs4953616
LHCGR ; STON1-GTF2A1L ; GTF2A1L
1.000 0.120 2 48714289 intron variant C/T snv 0.70 1
rs4844880
HSD11B1-AS1 ; HSD11B1
0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs6782041
LPP
1.000 0.120 3 188247396 intron variant T/C snv 0.70 1