Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17749155
MSRA
0.925 0.080 8 10210563 intron variant G/A snv 0.16 2
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs1247942 0.925 0.080 12 114235918 downstream gene variant G/A;C snv 2
rs2701108 0.925 0.160 12 114236456 downstream gene variant T/C snv 0.35 2
rs2409797
LINC00208
1.000 0.080 8 11576271 non coding transcript exon variant T/C;G snv 1
rs10108511
LINC00208
0.925 0.080 8 11578007 non coding transcript exon variant T/A;C snv 2
rs17451754
CFTR
0.925 0.080 7 117616658 intron variant G/A snv 0.10 2
rs3776082 1.000 0.080 5 150164482 upstream gene variant G/A;C snv 1
rs717746
CDX1
1.000 0.080 5 150176995 intron variant T/A;C;G snv 1
rs3776083
SLC6A7
1.000 0.080 5 150188407 upstream gene variant G/A;C;T snv 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 5
rs199620551
CRTC1
0.925 0.080 19 18693485 intron variant G/- del 9.2E-02 2
rs1548445
VPS35L
1.000 0.080 16 19680261 intron variant A/G snv 0.17 1
rs3072
GDF7
0.925 0.160 2 20678646 3 prime UTR variant T/C snv 0.30 2
rs7255
GDF7
0.925 0.080 2 20679060 3 prime UTR variant T/A;C snv 3
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135