Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5
rs10506481 0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
rs1475145065 0.882 0.080 14 24574706 missense variant C/G;T snv 4.0E-06; 8.0E-06 3
rs2972164 0.925 0.080 3 12292917 intron variant T/C snv 0.46 3
rs4684846 0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs6958571 0.925 0.080 7 30446094 intron variant A/C;G snv 1.2E-05; 0.25; 5.3E-05 3
rs773829498 0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06 3
rs77874543 0.882 0.080 22 41926712 missense variant G/C;T snv 6.1E-02 5.5E-02 3
rs11216153 0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs1153879 0.925 0.080 3 136392816 intron variant G/T snv 2
rs11666254 0.925 0.080 19 51759909 intron variant A/G snv 0.28 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
rs12605436 0.925 0.080 18 35906684 upstream gene variant C/T snv 9.1E-02 2
rs1419560997 0.925 0.080 11 117993410 splice region variant G/A snv 8.0E-06 7.0E-06 2
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs17602729 0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs1891320 0.925 0.080 1 19970618 upstream gene variant C/T snv 0.20 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
rs2715267 0.925 0.080 3 122052011 upstream gene variant G/A;T snv 2
rs2808530 0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs41279766 0.925 0.080 2 118970217 missense variant C/G;T snv 2.1E-03 2
rs4755453 0.925 0.080 11 36509094 intron variant C/A;G;T snv 2
rs497116 0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2