Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs12566888
PEAR1
0.807 0.280 1 156899255 intron variant G/T snv 0.26 7
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 7
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs4668123
LRP2
0.851 0.280 2 169196995 missense variant C/A;G;T snv 6
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
rs11573156
PLA2G2A
0.882 0.240 1 19979653 5 prime UTR variant G/C snv 0.19 5
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs4769874
ALOX5AP
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs8048002
LOC112267907 ; CIITA
0.851 0.320 16 10898131 intron variant T/A;C snv 4
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs1967309
ADCY9
0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs41273215
PEAR1
0.882 0.160 1 156912167 intron variant C/T snv 0.13 3