Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs1057156
RUVBL1
0.925 0.120 3 128081228 3 prime UTR variant A/G snv 0.22 0.23 2
rs149652370
RUVBL1
0.925 0.120 3 128084115 non coding transcript exon variant A/G snv 1.3E-04 2
rs7643459
LOC101927394 ; LMCD1-AS1
0.925 0.120 3 7963141 intron variant G/C;T snv 2
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs192876988
LOC105377300
0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 4
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs17329882
SYNPO2
0.925 0.120 4 119028805 intron variant A/C;T snv 2
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 3
rs237028
TAB2
0.925 0.120 6 149397514 intron variant C/T snv 0.58 2
rs2803073
PRKN
0.925 0.120 6 162541796 intron variant G/A snv 0.74 2
rs115344852
GPX6
1.000 0.120 6 28518321 intron variant A/C snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157