Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs1057519971
SPOP ; LOC107984999
1.000 0.080 17 49619326 missense variant T/C;G snv 2
rs1060501201
TP53
0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1197734477
PTEN
0.925 0.080 10 87961012 missense variant A/G snv 4
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913430
EGFR
1.000 0.080 7 55174740 missense variant G/A snv 3
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs138213197
HOXB13
0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs148609049
ANO7 ; LOC105373971
2 241188699 stop gained C/G;T snv 5.5E-03 1
rs1512268
LOC107986930
0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 6
rs1571801
DAB2IP
0.827 0.120 9 121665094 intron variant G/T snv 0.21 6
rs16861209
ADIPOQ
3 186845325 intron variant C/A;G snv 1
rs17366568
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs2155222 11 76642761 intergenic variant G/A;T snv 2
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs28909982
CHEK2
0.925 0.080 22 28725338 missense variant T/C snv 1.2E-04 9.1E-05 4
rs339331
RFX6
0.882 0.080 6 116888889 intron variant T/C snv 0.28 4
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs375118292
CUL3
0.925 0.080 2 224506080 missense variant T/A;C snv 2.0E-05 3
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32