Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201567874
TGFB1
1.000 0.080 19 41348412 missense variant C/T snv 6.8E-05 5.6E-05 3
rs115137622
HCG24 ; HLA-DPA3 ; LOC105375021
1.000 0.080 6 33143124 intron variant C/G snv 1
rs3132461 1.000 0.080 6 31512891 upstream gene variant G/A snv 0.84 1
rs408014
BLOC1S5-TXNDC5 ; TXNDC5
1.000 0.080 6 7899161 intron variant G/A snv 0.31 1
rs4396968
GABRB1
1.000 0.080 4 47087167 intron variant T/C snv 0.85 1
rs55859133
MAPK3
1.000 0.080 16 30116944 missense variant C/T snv 1.7E-03 1.4E-03 1
rs59661306
LUCAT1 ; ADGRV1
1.000 0.080 5 91087644 intron variant A/G snv 0.18 1
rs6547598
TCF7L1
1.000 0.080 2 85219363 intron variant A/G snv 0.26 1
rs6812281 1.000 0.080 4 179391655 intron variant T/A;G snv 1
rs73730372 1.000 0.080 6 32616804 regulatory region variant C/T snv 0.13 1
rs7457728
LINC01445
1.000 0.080 7 54380269 intron variant G/C snv 0.26 1
rs7771314
TXNDC5 ; BLOC1S5-TXNDC5
1.000 0.080 6 7891170 intron variant T/C snv 9.3E-02 1
rs9532669 1.000 0.080 13 40927414 downstream gene variant A/T snv 0.51 1
rs17102999
MLH3
0.925 0.120 14 75046831 missense variant G/A snv 1.3E-02 9.8E-03 2
rs997363
C2orf83
0.925 0.080 2 227644742 intron variant C/T snv 0.64 2
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 8
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 7
rs2566
LAMB3
0.882 0.080 1 209615169 3 prime UTR variant G/A snv 0.27 6
rs10802996
EXO1
0.882 0.080 1 241847325 upstream gene variant C/A;G snv 5
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 5
rs11568785
TGFBR1
0.882 0.080 9 99143552 intron variant A/G;T snv 7.2E-02 5
rs42033
CDK6
0.882 0.080 7 92608219 3 prime UTR variant A/T snv 0.16 5
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16 4
rs1474348
IL6-AS1 ; IL6
0.882 0.080 7 22728289 intron variant C/G snv 0.71 4
rs16970849
TMC8
0.882 0.080 17 78137827 intron variant G/A;T snv 0.11; 4.0E-06 4