Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs367737727
EVL
1.000 0.080 14 100128600 missense variant C/T snv 1.1E-05 1
rs773205136 1.000 0.080 2 100294302 missense variant G/A snv 4.1E-06 1
rs7849
SCD
1.000 0.080 10 100362846 3 prime UTR variant T/C;G snv 1
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs367898512 1.000 0.080 10 101002900 missense variant G/A snv 2.8E-05 7.0E-06 1
rs2281611 0.925 0.080 14 101033612 intron variant G/A;T snv 2
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs369664812 1.000 0.080 7 101223799 missense variant C/T snv 2.8E-05 4.2E-05 1
rs34713741 0.882 0.280 15 101277671 upstream gene variant C/A;T snv 0.24 3
rs1419316960 0.925 0.080 19 10166651 missense variant T/C snv 7.0E-06 2
rs2186607 0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs823920 0.925 0.080 9 101900303 intergenic variant A/G snv 0.12 2
rs990101456 1.000 0.080 10 102109138 missense variant C/T snv 1
rs537292284 1.000 0.080 10 102133102 missense variant G/C snv 1
rs35060588 0.925 0.080 3 10213318 missense variant C/G;T snv 5.5E-02; 1.6E-05 2
rs1215486792
MOK
0.925 0.080 14 102229572 missense variant C/G snv 7.0E-06 2
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1287689842 1.000 0.080 7 102281843 missense variant C/T snv 7.0E-06 1
rs11704 0.925 0.080 14 102342318 3 prime UTR variant G/C snv 0.26 2
rs2946834 0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26