Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs200182588 0.827 0.160 9 104094409 5 prime UTR variant -/GC ins 7.0E-06 6
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs267607911 0.851 0.200 2 47403192 start lost A/C;G;T snv 5.1E-05; 1.4E-05 8
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1467465 0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs1469713 0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs181206 0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101