Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1248696
DLG5
0.807 0.080 10 77856847 missense variant T/A;C snv 0.93 8
rs1545620
MYO9B
0.827 0.080 19 17192965 missense variant T/A;G snv 1.3E-05; 0.52 6
rs10883365
LINC01475
0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 3
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 3
rs888208
NKX2-3
0.882 0.080 10 99536106 3 prime UTR variant A/G snv 0.25 3
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs10491434
IL7R
1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 2
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 2
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 2
rs2041570
LOC107986781
0.925 0.080 7 31159653 intergenic variant G/A snv 0.50 2
rs2762051
DLEU1
1.000 0.080 13 50261579 intron variant C/T snv 0.15 2
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 2
rs936229
ULK3
1.000 0.080 15 74839978 intron variant A/G snv 0.67 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs1018326
LINC01934
1.000 0.080 2 181143073 intron variant T/C snv 0.47 1
rs1033180 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 1
rs10484718
THEMIS
1.000 0.080 6 127859906 intron variant A/T snv 8.6E-02 1
rs10796045 1.000 0.080 10 6360779 intergenic variant G/T snv 0.79 1
rs10800746
INAVA
1.000 0.080 1 200912264 intron variant C/T snv 0.32 1
rs10886159 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 1
rs11100722 1.000 0.080 4 141616307 intergenic variant G/C snv 0.77 1
rs11734090
KIAA1109
1.000 0.080 4 122306958 intron variant T/C snv 0.25 1