Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4954218
MAP3K19
0.925 0.080 2 135045855 intron variant G/T snv 0.83 5
rs9938149 0.925 0.160 16 88298034 intron variant C/A snv 0.66 4
rs6445055
FNDC3B
0.925 0.040 3 172274597 intron variant G/A snv 0.24 4
rs1536482 1.000 0.040 9 134548682 upstream gene variant G/A snv 0.36 3
rs2721051 1.000 0.040 13 40536747 intron variant C/T snv 8.6E-02 3
rs12447690
LOC107984862
1.000 0.160 16 88264518 intron variant C/T snv 0.53 3
rs7677751
PDGFRA
0.925 0.040 4 54258293 intron variant C/T snv 0.18 3
rs10453441
WNT7B
1.000 0.040 22 45967859 intron variant A/G snv 0.40 3
rs11616662 13 40545329 intron variant G/A snv 0.11 2
rs12448211 16 88296907 intron variant G/A snv 0.56 2
rs1324183 1.000 0.040 9 13557492 intron variant A/C;T snv 2
rs2114039 1.000 0.080 4 54226459 intron variant T/C snv 0.40 2
rs3118520 9 134549749 upstream gene variant A/G snv 0.49 2
rs4792535 17 14661813 intergenic variant C/T snv 0.45 2
rs4938174 11 111042516 upstream gene variant G/A snv 0.31 2
rs6540223 16 88287830 intron variant C/T snv 0.72 2
rs7040970 9 136964561 upstream gene variant T/C snv 0.44 2
rs8111998 1.000 0.040 19 22558873 downstream gene variant C/T snv 0.23 2
rs4948502
ARID5B
1.000 0.040 10 62079658 intron variant T/C snv 0.33 2
rs752092
CHSY1
15 101241729 intron variant A/G snv 0.43 2
rs7606754
COL4A3 ; MFF-DT
1.000 0.040 2 227270464 intron variant A/G snv 0.69 2
rs7044529
COL5A1
1.000 0.040 9 134676205 intron variant C/T snv 0.21 2
rs96067
COL8A2
1 36106319 intron variant G/A snv 0.73 2
rs4894535
FNDC3B
1.000 0.040 3 172277815 intron variant C/A;T snv 2
rs2755237
LINC00598
13 40535292 intron variant A/C snv 0.17 2