Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs526934
TCN1
0.925 0.080 11 59866020 intron variant G/A snv 0.77 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs3734254
PPARD
0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 1
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 9
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 3
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 2
rs3793964
TOLLIP
0.882 0.120 11 1280752 intron variant T/C snv 0.66 1
rs3180235
IL36RN
0.882 0.080 2 113063095 3 prime UTR variant A/G snv 0.65 1
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 1
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 2
rs869736
CORO1B ; PTPRCAP
0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53 1
rs11869286
STARD3
0.925 0.080 17 39657603 intron variant G/C snv 0.52 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs1877031
STARD3
0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52 2
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6