Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs6031431
JPH2
20 44166512 intron variant A/G snv 0.46 4
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs8126001
RGS19 ; OPRL1
20 64080106 5 prime UTR variant C/T snv 0.46 4
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 3
rs1239948
DLEU1 ; DLEU7
13 50532386 intron variant A/T snv 0.59 3
rs1883711 20 40551182 regulatory region variant G/C snv 2.5E-02 3
rs2760061 1 228003374 upstream gene variant T/A snv 0.55 3
rs35479618
MIR8083 ; NPR1
1 153689947 missense variant G/A snv 9.5E-03 1.1E-02 3
rs3821843
CACNA1D
3 53523985 intron variant G/A snv 0.72 3
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73 3
rs612652
LSP1
11 1865986 intron variant T/C snv 0.55 3
rs6441207
LOC100996447
3 158564670 intron variant C/T snv 0.45 3
rs6787344 3 186622052 intron variant G/C snv 0.19 3
rs687914
PRKCE ; LOC102724965
2 45651621 5 prime UTR variant G/A;T snv 3
rs7134677
HOXC4
12 54047714 intron variant C/T snv 0.29 3
rs72656645
APOLD1 ; LOC107984129
12 12728121 intron variant A/G snv 0.21 3
rs72801474 5 133108436 downstream gene variant G/A snv 5.2E-02 3
rs73033340
ZFAND2A
7 1156056 intron variant A/G snv 2.7E-02 3
rs74439044
NAA38
17 7877701 intron variant T/C snv 8.9E-02 3
rs76452347
HRCT1
9 35906474 missense variant C/G;T snv 0.15 0.16 3
rs893929 4 143266227 intergenic variant G/A snv 0.42 3
rs9321485 6 135126635 intergenic variant T/C snv 0.29 3