Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs563558831
CYP2B6
0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs2155209
MRE11
0.776 0.240 11 94417624 3 prime UTR variant T/C snv 0.27 10
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1314386070
DECR1
0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs773297988
PIK3CB
0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4
rs12347433
DELEC1 ; TNC
0.882 0.040 9 115035318 synonymous variant T/C snv 0.23 0.21 3
rs212528
ECE1
0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs2269422
AGER
0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3
rs28937313
ABCA1
0.882 0.160 9 104822520 missense variant T/C snv 8.0E-06 3
rs746481995
HSD11B1 ; HSD11B1-AS1
0.882 0.120 1 209707123 missense variant T/C snv 4.0E-06 3
rs8070488
HGS
0.882 0.080 17 81696901 synonymous variant T/C snv 0.21 0.26 3
rs13447720
MRE11
0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs4901536
SAMD4A
0.925 0.080 14 54733816 intron variant T/C snv 0.67 2
rs767523236
MPO
0.925 0.040 17 58279033 missense variant T/C snv 4.1E-06 7.0E-06 2
rs915014
C1orf167 ; MTHFR
0.925 0.040 1 11789412 missense variant T/C snv 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs879254693
LDLR
0.807 0.160 19 11107424 missense variant T/A;C;G snv 7