Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010159 0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs10119 0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs10407447 1.000 0.040 19 40363275 intron variant A/G snv 0.20 1
rs104894103 0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs111943087 0.925 0.080 5 150059725 missense variant G/A snv 1.4E-05 2
rs11218304 0.925 0.080 11 121478402 intron variant A/G snv 0.30 2
rs1130399 1.000 0.040 6 32661978 missense variant G/A;T snv 0.20 1
rs11556510 1.000 0.040 19 44891562 missense variant T/G snv 9.8E-03 1.2E-02 1
rs11637611 0.851 0.160 15 72259371 intron variant C/T snv 0.63 4
rs11667768 1.000 0.040 19 40348525 5 prime UTR variant C/T snv 6.3E-02 0.11 1
rs11767557 0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs11887120 0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs12053868 0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12344615 0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs12752888 0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 4
rs1334496 1.000 0.040 X 137178554 intergenic variant C/A;T snv 1
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1451603364 0.925 0.120 11 27658411 missense variant C/T snv 4.0E-06 2
rs15009 0.925 0.080 5 58454523 3 prime UTR variant C/G snv 0.37 2
rs157581 0.925 0.080 19 44892457 synonymous variant T/C snv 0.25 0.29 3