Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6444174
ADIPOQ-AS1 ; ADIPOQ
1.000 0.080 3 186855400 3 prime UTR variant C/T snv 0.95 1
rs11647470 1.000 0.080 16 55157878 intergenic variant C/T snv 0.93 1
rs4969169
SOCS3
1.000 0.080 17 78357829 3 prime UTR variant T/C snv 0.92 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs2885373
IL1RAP
1.000 0.080 3 190628679 intron variant T/C snv 0.90 1
rs2669845
CX3CR1
0.925 0.120 3 39279727 intron variant T/C snv 0.87 2
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs3809508
WDR73 ; NMB
1.000 0.080 15 84655660 intron variant T/C snv 0.86 1
rs2721
LOC105375591 ; INSIG1
1.000 0.080 7 155296033 non coding transcript exon variant T/G snv 0.85 1
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 4
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 4
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 2
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs1109859
PEMT
1.000 0.080 17 17521019 intron variant G/A snv 0.83 1
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs1956549
C14orf39
1.000 0.080 14 60461483 intron variant G/A snv 0.87 0.82 1
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs3745318
KLF2
1.000 0.080 19 16325451 missense variant T/C snv 0.75 0.82 2
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs7431368
DNAJB8-AS1
1.000 0.080 3 128472098 non coding transcript exon variant C/A snv 0.82 1