Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3132461 1.000 0.080 6 31512891 upstream gene variant G/A snv 0.84 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
rs9532669 1.000 0.080 13 40927414 downstream gene variant A/T snv 0.51 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
rs115137622
HCG24 ; HLA-DPA3 ; LOC105375021
1.000 0.080 6 33143124 intron variant C/G snv 1
rs7457728
LINC01445
1.000 0.080 7 54380269 intron variant G/C snv 0.26 1
rs59661306
LUCAT1 ; ADGRV1
1.000 0.080 5 91087644 intron variant A/G snv 0.18 1
rs55859133
MAPK3
1.000 0.080 16 30116944 missense variant C/T snv 1.7E-03 1.4E-03 1
rs6547598
TCF7L1
1.000 0.080 2 85219363 intron variant A/G snv 0.26 1
rs7771314
TXNDC5 ; BLOC1S5-TXNDC5
1.000 0.080 6 7891170 intron variant T/C snv 9.3E-02 1
rs997363
C2orf83
0.925 0.080 2 227644742 intron variant C/T snv 0.64 2
rs17102999
MLH3
0.925 0.120 14 75046831 missense variant G/A snv 1.3E-02 9.8E-03 2
rs1195571 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 3
rs180082 0.882 0.080 17 69955727 intergenic variant C/G;T snv 3
rs9302648
AKTIP
0.882 0.080 16 53493869 non coding transcript exon variant G/T snv 0.54 3
rs5757465
APOBEC3G
0.882 0.080 22 39081118 synonymous variant T/C snv 0.37 0.31 3
rs3744935
BCL2
0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03 3
rs11079454
BRIP1
0.882 0.080 17 61679808 3 prime UTR variant T/A;C snv 3
rs16945692
BRIP1
0.882 0.080 17 61862883 intron variant A/G snv 0.17 3
rs42032
CDK6
0.882 0.080 7 92608112 3 prime UTR variant G/A snv 0.28 3
rs4777498
CELF6
0.882 0.080 15 72285731 3 prime UTR variant C/A snv 0.74 3
rs17885289
CXCL12
0.882 0.080 10 44386212 non coding transcript exon variant C/T snv 0.26 3
rs266093
CXCL12
0.882 0.080 10 44370760 3 prime UTR variant C/G;T snv 3