Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25655
CAPN2
0.925 0.080 1 223712706 missense variant C/G snv 1.00 0.99 2
rs2788612
KCND3
1.000 0.080 1 111873741 intron variant T/C snv 0.96 1
rs156113 0.925 0.080 6 104369868 intergenic variant A/T snv 0.96 2
rs2665582
SULT2B1
0.925 0.080 19 48584410 intron variant T/C snv 0.94 2
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs7837688 0.925 0.080 8 127527115 intergenic variant T/G snv 0.91 2
rs9915936
AXIN2
0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs1534891
CSNK1E ; TPTEP2-CSNK1E
0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs851023
MAPK14
0.925 0.080 6 36038443 intron variant G/A snv 0.89 2
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 3
rs1456305
CASC19 ; PCAT1
1.000 0.080 8 127115007 intron variant G/A snv 0.88 1
rs8041922
ALDH1A2
0.925 0.080 15 57983978 intron variant C/A;G snv 0.88 2
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs554518
LOC105376622
0.882 0.080 11 34434641 upstream gene variant T/C snv 0.87 3
rs11125927 1.000 0.080 2 62525840 regulatory region variant G/A snv 0.86 1
rs822391
ADIPOQ
0.925 0.080 3 186846014 intron variant C/T snv 0.85 4
rs1881502
MOB2
1.000 0.080 11 1486282 intron variant T/C snv 0.85 1
rs11649743
LOC105371754 ; HNF1B
0.925 0.080 17 37714971 intron variant A/G snv 0.85 2
rs2659124
LOC105372441
1.000 0.080 19 50851341 upstream gene variant A/T snv 0.84 1
rs895521
NPAS2
0.925 0.080 2 100935633 intron variant T/C snv 0.84 2
rs35605
ABCC1
0.925 0.080 16 16068162 synonymous variant T/C snv 0.79 0.84 2
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6