Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10242177 1.000 0.120 7 156369656 intergenic variant C/A;T snv 1
rs1528845 1.000 0.120 2 147749295 intergenic variant T/C;G snv 1
rs2325377 1.000 0.120 13 71321166 intergenic variant C/T snv 0.99 1
rs74819164 1.000 0.120 2 147748280 intergenic variant A/G snv 7.0E-02 1
rs143238378
LINC02476
1.000 0.120 7 119626216 intron variant G/A;T snv 1
rs150382487
LINC02476
1.000 0.120 7 119500548 intron variant T/A snv 2.4E-03 1
rs182830500
LINC02476
1.000 0.120 7 119521299 intron variant T/C snv 2.6E-03 1
rs188681640
LINC02476
1.000 0.120 7 119506105 intron variant A/G snv 2.4E-03 1
rs113691307
LOC102724542
1.000 0.120 2 81801266 intergenic variant C/T snv 6.1E-02 1
rs80004662
LOC102724542
1.000 0.120 2 81798061 intergenic variant A/G snv 6.1E-02 1
rs2405373
LOC105376157
1.000 0.120 9 95549844 intergenic variant G/A snv 0.32 1
rs28434654
LOC105376157
1.000 0.120 9 95524196 intergenic variant A/G snv 0.28 1
rs28637199
LOC105376157
1.000 0.120 9 95532166 intergenic variant T/G snv 0.29 1
rs28689133
LOC105376157
1.000 0.120 9 95531283 intergenic variant A/C;G snv 0.28 1
rs3847316
LOC105376157
1.000 0.120 9 95532733 intergenic variant T/C snv 0.29 1
rs3858092
LOC105376157
1.000 0.120 9 95529166 regulatory region variant A/C snv 0.29 1
rs11597348
OPALIN
1.000 0.120 10 96354046 intron variant A/T snv 7.9E-02 1
rs12175475
PRKN
1.000 0.120 6 162250424 intron variant A/T snv 2.1E-02 1
rs189675673
SULT2A1
1.000 0.120 19 47880143 intron variant G/A;T snv 1
rs62529857
SULT2A1
1.000 0.120 19 47883216 intron variant T/C snv 7.7E-03 1
rs117496742
YAP1
1.000 0.120 11 102208982 intron variant G/A;T snv 1.3E-02 1
rs10462065 0.925 0.120 5 44068744 upstream gene variant C/A snv 8.3E-02 2
rs12375983 0.925 0.120 9 89595154 intron variant G/A snv 0.13 2
rs1243572 0.925 0.120 14 94913162 intergenic variant T/C snv 0.78 2
rs1873147 0.925 0.120 15 63020433 regulatory region variant G/A snv 0.66 2