Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1291621
SCAF11
1.000 0.040 12 45947038 intron variant A/G snv 0.98 1
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs3130683
C2 ; CYP21A2
1.000 0.040 6 31920590 intron variant C/T snv 0.91 1
rs9380586 1.000 0.040 6 36663787 regulatory region variant A/G;T snv 0.91 1
rs12493885
ARHGEF26-AS1 ; ARHGEF26
1.000 0.040 3 154122077 missense variant G/C snv 0.91 0.91 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs1629862
EDN1
1.000 0.040 6 12295643 intron variant A/G snv 0.89 1
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs430918 1.000 0.040 6 57249018 intergenic variant C/T snv 0.87 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs1024610 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 3
rs253662
MRAS
1.000 0.040 3 138378471 intron variant T/C snv 0.84 1
rs2475376
CYP2C9
1.000 0.040 10 94952643 intron variant A/G snv 0.84 1
rs7797644
KDELR2 ; DAGLB
1.000 0.040 7 6446436 intron variant T/C snv 0.84 1
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs11859599
MPHOSPH6
1.000 0.040 16 82149227 intron variant C/G snv 0.83 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2257129
LOC105378522
1.000 0.040 10 121139183 regulatory region variant T/C snv 0.82 3
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 4