Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs333
CCR5 ; CCR5AS
0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs2107538
LOC105371744 ; CCL5
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 11
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6