Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11150612 1.000 0.120 16 31346439 intergenic variant G/A snv 0.28 1
rs12716641 1.000 0.120 8 7041476 upstream gene variant T/A;C snv 1
rs1369270 1.000 0.120 2 153179546 intron variant T/C snv 1
rs2033562 1.000 0.120 8 102535511 intron variant G/A;C;T snv 1
rs2615787 1.000 0.120 8 6953627 upstream gene variant T/G snv 0.41 1
rs2738048 1.000 0.120 8 6965263 downstream gene variant A/G snv 0.28 1
rs2738081 1.000 0.120 8 6957996 downstream gene variant G/T snv 0.15 1
rs3129269 1.000 0.120 6 33129837 downstream gene variant C/A;T snv 1
rs4288398 1.000 0.120 8 7024116 downstream gene variant A/G snv 0.70 1
rs6984215 1.000 0.120 8 7027356 downstream gene variant T/C snv 0.30 1
rs7763262 1.000 0.120 6 32457105 downstream gene variant T/C snv 0.70 1
rs2074038 1.000 0.120 11 44066439 5 prime UTR variant G/T snv 8.4E-02 1
rs887280103
ACE
1.000 0.120 17 63477294 missense variant C/G snv 1.4E-05 1
rs2296136 1.000 0.120 10 5887999 missense variant G/C;T snv 5.3E-02 1
rs2072392
BID
1.000 0.120 22 17743846 synonymous variant A/G snv 2.8E-02 4.1E-02 1
rs1008898 1.000 0.120 7 7233928 intron variant G/A;T snv 1
rs5882115 1.000 0.120 7 7233965 intron variant -/C delins 7.6E-02 1
rs761991666 1.000 0.120 7 7234516 missense variant A/G snv 4.0E-06 7.0E-06 1
rs7790522 1.000 0.120 7 7242918 intron variant A/G snv 0.30 1
rs2227543 1.000 0.120 4 73742193 3 prime UTR variant C/T snv 0.32 1
rs11084377 1.000 0.120 19 54875434 intron variant A/G;T snv 1
rs11264793 1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28 1
rs6691569 1.000 0.120 1 157678308 3 prime UTR variant G/A snv 0.24 1
rs10488764 1.000 0.120 11 110460907 intron variant G/A snv 0.18 1
rs637571 1.000 0.120 11 65896875 synonymous variant T/C snv 0.51 0.50 1