Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6550253
LINC01811
1.000 0.120 3 34149739 intron variant G/A snv 0.12 3
rs72772090
CAST
1.000 0.120 5 96700607 intron variant G/A;C snv 3
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3
rs7818688
NDUFAF6
1.000 0.120 8 95011854 intron variant C/A;G snv 3
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 2
rs11155133
LOC102723724
0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 2
rs2089222
MAP1LC3B2
0.925 0.200 12 116564853 intron variant G/A snv 0.12 2
rs2191566
ZNF230
0.925 0.200 19 44007237 intron variant G/T snv 0.62 2
rs2242041
FIGNL1 ; DDC
0.925 0.120 7 50461751 intron variant C/G snv 7.7E-02 2
rs3887825
DDC ; FIGNL1
1.000 0.120 7 50477395 intron variant T/C snv 0.56 2
rs442767
MSH3 ; DHFR
0.925 0.120 5 80655677 intron variant G/T snv 0.27 2
rs4947584
FIGNL1 ; DDC
1.000 0.120 7 50505011 intron variant A/T snv 0.35 2
rs7896246
ARID5B
0.925 0.120 10 61964631 intron variant A/G snv 0.74 2
rs1037351
FIGNL1 ; DDC
1.000 0.120 7 50497706 intron variant T/C snv 0.30 1
rs10899736
DDC ; FIGNL1
1.000 0.120 7 50479227 intron variant G/A;C snv 1
rs11013046
PIP4K2A
1.000 0.120 10 22551654 intron variant C/T snv 0.55 1
rs11575387
FIGNL1 ; DDC
1.000 0.120 7 50499737 intron variant T/A;G snv 1
rs11575575
FIGNL1
1.000 0.120 7 50456510 intron variant C/A snv 7.5E-02 1
rs12719039
IKZF1
1.000 0.120 7 50351251 intron variant T/C snv 0.25 1
rs17133853
FIGNL1 ; DDC
1.000 0.120 7 50501717 intron variant A/G snv 0.12 1
rs17152020
FIGNL1 ; DDC
1.000 0.120 7 50482161 intron variant T/A snv 0.22 1
rs17505102
TP63
1.000 0.120 3 189683987 intron variant G/C snv 9.7E-02 1
rs2069426
CDKN2B ; CDKN2B-AS1
1.000 0.120 9 22006274 intron variant G/A;C;T snv 4.4E-06; 4.4E-06; 7.5E-02 1
rs207954
SLCO3A1
1.000 0.120 15 92114143 intron variant T/A;C;G snv 1
rs2167364
DDC ; FIGNL1
1.000 0.120 7 50498129 intron variant T/C snv 0.30 1