Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6