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
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs9915936
AXIN2
0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs2740348
GEMIN4
0.851 0.160 17 746695 missense variant G/C;T snv 0.85 6
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs35605
ABCC1
0.925 0.080 16 16068162 synonymous variant T/C snv 0.79 0.84 2
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs1047303
HSD3B1
0.851 0.120 1 119514623 missense variant C/A snv 0.75 4
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 3
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs3208008
RTEL1 ; TNFRSF6B ; RTEL1-TNFRSF6B
0.925 0.080 20 63694757 missense variant A/C snv 0.75 0.81 2
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs9666607
CD44
0.925 0.080 11 35204608 missense variant A/G;T snv 0.74 2
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 9
rs11781886
NKX3-1 ; LOC107986930
0.925 0.080 8 23682904 5 prime UTR variant C/T snv 0.72 0.72 2
rs2274911
GPRC6A
0.851 0.160 6 116809541 missense variant G/A snv 0.72 0.74 6
rs2660
OAS1
0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75 4
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2287939
AMACR ; C1QTNF3-AMACR
0.851 0.160 5 33998778 missense variant A/C;G snv 1.6E-05; 0.70 4
rs2305745
HPN-AS1 ; HPN
0.925 0.080 19 35065377 intron variant G/A snv 0.70 0.63 2
rs2278008
C1QTNF3-AMACR ; AMACR
0.851 0.160 5 33989413 missense variant C/T snv 0.70 0.74 4
rs2292912
CRY2
0.851 0.120 11 45856137 non coding transcript exon variant C/A;G;T snv 8.0E-06; 0.69 4
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92