Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10421916
INSL3
0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs154268
PRKAA1
0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs2231231
AQP3
0.851 0.240 9 33442988 non coding transcript exon variant A/C snv 0.67 0.69 5
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs3734254
PPARD
0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs4626
TOB1
0.925 0.080 17 50863061 synonymous variant T/C snv 0.66 0.69 2
rs2643194
ERBB2 ; PGAP3
0.925 0.080 17 39696795 5 prime UTR variant C/T snv 0.67 2
rs121224
MIR365B ; MIR4725
0.851 0.080 17 31574981 intron variant G/C snv 0.66 4
rs2934971
ERBB2
0.925 0.080 17 39698254 intron variant G/T snv 0.66 2
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs4796030
LIG3
0.827 0.120 17 35003131 3 prime UTR variant A/C snv 0.66 6
rs734004
EZH2
0.925 0.080 7 148808368 intron variant G/C snv 0.66 2
rs3793964
TOLLIP
0.882 0.120 11 1280752 intron variant T/C snv 0.66 4
rs3180235
IL36RN
0.882 0.080 2 113063095 3 prime UTR variant A/G snv 0.65 3
rs2472188
IL36RN
0.925 0.080 2 113063237 3 prime UTR variant C/G snv 0.65 2
rs957201
IL36RN
0.925 0.080 2 113063623 3 prime UTR variant T/C snv 0.65 2
rs2515402
IL36RN
0.925 0.080 2 113063003 3 prime UTR variant C/A snv 0.65 2
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs882537
PADI4
1.000 0.080 1 17333552 intron variant A/G snv 0.64 1
rs184432
TFF1
0.882 0.120 21 42367453 upstream gene variant G/A snv 0.64 3
rs3774968
NFKB1 ; LOC105377347
0.882 0.120 4 102609955 intron variant A/G snv 0.64 4