Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9529561 1.000 0.080 13 69325374 downstream gene variant A/G snv 6.3E-02 1
rs58764888 1.000 0.080 3 11176005 intron variant T/A snv 5.8E-02 1
rs945177 1.000 0.080 13 27047848 intergenic variant G/A;T snv 1
rs150062338
LPP
1.000 0.080 3 188287160 intron variant C/T snv 3.6E-02 1
rs117983287 1.000 0.080 9 77405958 missense variant C/A snv 9.6E-03 8.3E-03 1
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs1891320 0.925 0.080 1 19970618 upstream gene variant C/T snv 0.20 2
rs11684747 0.925 0.080 2 9557042 upstream gene variant A/G snv 0.19 2
rs11689958 0.925 0.080 2 9557277 upstream gene variant G/A snv 0.19 2
rs17602729 0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs11216153 0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs506027 0.925 0.080 6 106326589 upstream gene variant G/A snv 0.57 2
rs497116 0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2
rs1915087 0.925 0.080 3 122119944 3 prime UTR variant T/C snv 2
rs2332096 0.925 0.080 3 122102296 intron variant T/A;G snv 2
rs11666254 0.925 0.080 19 51759909 intron variant A/G snv 0.28 2
rs2808530 0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs1419560997 0.925 0.080 11 117993410 splice region variant G/A snv 8.0E-06 7.0E-06 2
rs2715267 0.925 0.080 3 122052011 upstream gene variant G/A;T snv 2
rs41279766 0.925 0.080 2 118970217 missense variant C/G;T snv 2.1E-03 2
rs12605436 0.925 0.080 18 35906684 upstream gene variant C/T snv 9.1E-02 2
rs1153879 0.925 0.080 3 136392816 intron variant G/T snv 2
rs595209 0.925 0.080 11 126292326 intron variant A/C;G snv 2
rs8177375 0.925 0.080 11 126293169 3 prime UTR variant A/G snv 0.12 0.13 2
rs5744105 0.925 0.080 1 223142735 intron variant G/C snv 0.57 2