Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704397
PDE8B
0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs2046045
PDE8B
0.925 0.080 5 77239986 intron variant T/C;G snv 4
rs6885099
PDE8B
1.000 0.040 5 77234524 intron variant A/G snv 0.52 4
rs3813582
LINC01229 ; LOC105371356 ; MAFTRR
16 79715456 non coding transcript exon variant T/C snv 0.28 3
rs12138950
LOC105376817 ; LOC105376819 ; LOC105376818 ; MICOS10
0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 3
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs1382879
PDE8B
1.000 0.040 5 77226043 intron variant T/A;C snv 3
rs11935941
LOC107986195
1.000 0.040 4 148731326 intron variant A/C snv 0.31 2
rs10917477
MICOS10
1.000 0.040 1 19534612 intron variant A/C;G;T snv 2
rs10036386
PDE8B
1.000 0.040 5 77247778 intron variant C/T snv 0.40 2
rs1479567
PDE8B
1.000 0.040 5 77232197 intron variant G/A;C snv 2
rs13401647 2 204192945 intergenic variant T/C;G snv 0.19 1
rs1908679 12 69084258 intergenic variant G/A;C snv 1
rs10493251
DAB1
1 58298409 intron variant C/T snv 0.23 1
rs11576201
DAB1
1 58290976 intron variant G/A snv 0.23 1
rs4334315
LINC01229 ; LOC105371356 ; MAFTRR
16 79722300 intron variant A/T snv 0.27 1
rs211811
LOC105375451 ; LOC105375450
7 110443615 intron variant A/G;T snv 1
rs568931048
LOC105376818 ; MICOS10 ; LOC105376817 ; LOC105376819
1 19512621 intron variant -/AAACA;AACA;AACAAAACA;AACAAAACAAAACA delins 1
rs4394682
LOC105376818 ; MICOS10 ; LOC105376819
1 19511043 intron variant A/G snv 0.20 1
rs11806434
LOC105376819 ; MICOS10
1 19505943 intron variant G/A snv 0.20 1
rs11807599
LOC105376819 ; MICOS10
1 19505445 intron variant C/T snv 0.22 1
rs16822442
LOC105376819 ; MICOS10
1 19501476 intron variant A/G snv 0.19 1
rs2745217
LOC105378614 ; MICOS10-NBL1 ; MICOS10
1 19595253 intron variant C/T snv 0.64 1
rs10002630
LOC107986195
4 148737523 intron variant G/C snv 0.31 1