Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs563558831
CYP2B6
0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs2155209
MRE11
0.776 0.240 11 94417624 3 prime UTR variant T/C snv 0.27 10
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs6903956
ADTRP
0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1314386070
DECR1
0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs46522
UBE2Z
0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs879254925
MIR6886 ; LDLR
0.790 0.120 19 11113680 missense variant G/T snv 8
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs16933090
SOX6
0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7