Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3755397
FARP2
0.925 0.120 2 241355498 upstream gene variant A/G snv 6.8E-02 4
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 3
rs35923643
GRAMD1B
0.925 0.120 11 123484683 intron variant A/G snv 0.15 3
rs4987852
BCL2
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02 3
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv 3
rs1036935 0.925 0.120 18 50317164 upstream gene variant A/G;T snv 2
rs1044873
IRF8
0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 2
rs11636802
LOC105370831
0.925 0.120 15 56483399 intergenic variant A/G snv 8.0E-02 2
rs11637565
DRAIC
0.925 0.120 15 69728186 intron variant G/A snv 0.66 2
rs1274963
CSRNP1
0.925 0.120 3 39149538 non coding transcript exon variant A/G snv 0.82 2
rs13015798
FAM126B
0.925 0.120 2 201044792 intron variant A/G snv 0.23 2
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 2
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 2
rs140099016
CASC19 ; PCAT1
0.925 0.120 8 127183089 intron variant T/C snv 2
rs142215530
LOC105370831
0.925 0.120 15 56485493 intergenic variant A/G snv 8.0E-02 2
rs1439287
ACOXL-AS1 ; ACOXL ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 2
rs1476569 0.925 0.120 4 113777540 intergenic variant A/G snv 0.34 2
rs16976734
RFX7
0.925 0.120 15 56090097 3 prime UTR variant A/G snv 0.12 2
rs17246404
POT1
0.925 0.120 7 124822607 3 prime UTR variant C/A;T snv 2
rs2003869
LEF1
0.925 0.120 4 108105258 intron variant A/C;G;T snv 2
rs2052702
DRAIC
0.925 0.120 15 69697166 non coding transcript exon variant A/C;T snv 2
rs2236256
IPCEF1 ; OPRM1
0.925 0.120 6 154157305 3 prime UTR variant C/A snv 0.52 2
rs2267708
GPR37
0.925 0.120 7 124752458 intron variant C/T snv 0.47 2
rs2396718
SP110
0.925 0.120 2 230179539 intron variant T/C snv 6.7E-02 2
rs2466029
CASC19 ; PCAT1
0.925 0.120 8 127188726 non coding transcript exon variant C/G;T snv 2