Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786205228
PPP2R1A
0.827 0.080 19 52212718 missense variant C/G;T snv 6
rs11196418
CASP7
0.925 0.080 10 113678707 upstream gene variant G/A snv 0.11 4
rs117039649
MDM2
0.925 0.080 12 68808776 intron variant G/C snv 2.3E-02 4
rs149308960
ESR1
0.925 0.080 6 151842622 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 1.6E-03 4
rs1694964
LINC02025
0.925 0.080 3 84885341 intron variant G/T snv 4
rs8135424
CHEK2
0.925 0.080 22 28689804 intron variant G/A snv 0.14 4
rs1045242
TNFAIP8
0.925 0.080 5 119393632 3 prime UTR variant A/G snv 0.32 3
rs1156807933
MAX ; LOC100506321
0.925 0.080 14 65093799 missense variant T/C snv 4.0E-06 3
rs12112075
OGDH
0.925 0.080 7 44609201 intron variant G/A snv 1.8E-02 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3
rs2453839
IGFBP3
0.925 0.080 7 45913974 intron variant T/C snv 0.26 3
rs2475335
PTPRD
0.882 0.080 9 10260263 intron variant C/A;T snv 3
rs4980524
STIP1
0.882 0.080 11 64191787 intron variant A/C;T snv 3
rs10502289
ENOSF1
0.925 0.080 18 676789 intron variant A/T snv 0.15 2
rs10733710
TGFBR1
0.925 0.080 9 99145142 intron variant G/A snv 0.21 2
rs11196445
CASP7
0.925 0.080 10 113710131 intron variant G/A snv 0.11 2
rs11224561
PGR
0.925 0.080 11 101034325 3 prime UTR variant C/A;T snv 2
rs1182154114
SULT1A1
0.925 0.080 16 28623160 missense variant G/C snv 2
rs1337082
LOC105373241
0.925 0.080 X 67764173 intergenic variant G/A snv 0.61 2
rs140296720
DDR1
0.925 0.080 6 30896816 missense variant G/A snv 4.3E-06 2
rs1438956733
FGFR2
0.925 0.080 10 121515180 synonymous variant G/A snv 7.0E-06 2
rs1740828 0.925 0.080 6 21648854 regulatory region variant G/A snv 0.55 2
rs201768983
TNK2
0.925 0.080 3 195868640 missense variant C/T snv 1.2E-04 3.5E-05 2
rs2298581
ENOSF1
0.925 0.080 18 677931 intron variant C/G snv 0.22 2