Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs567798234
AMPD2
0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs2293489
BUD23
0.925 0.120 7 73692949 non coding transcript exon variant C/T snv 0.26 2
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs33972313
SLC23A1
0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 8
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs752596535
LDLR
0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs4717806
LOC105375350 ; STX1A ; BUD23
0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs6749704
CCL20
0.827 0.240 2 227813126 intron variant T/C snv 0.24 5
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22