Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs220733
MAS1
1.000 0.080 6 159897771 intron variant A/C;G snv 0.99 3
rs6565564
BAHCC1
17 81408117 intron variant G/C snv 0.96 1
rs3735533
HOTTIP
7 27206274 non coding transcript exon variant T/C snv 0.93 4
rs10748798
PAX2
10 100794914 intron variant C/T snv 0.91 1
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs13190036
MXD3
5 177310719 non coding transcript exon variant A/G snv 0.83 0.89 1
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs1406961
NKAIN4
20 63264568 intron variant A/C snv 0.87 2
rs134557
C22orf31
22 29061594 intron variant A/G;T snv 0.84 1
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs324175
LOC105376587 ; ANO5 ; LOC102723370
11 21932141 intron variant T/C snv 0.83 1
rs562556
PCSK9
0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs133049
MRTFA
0.882 0.080 22 40635351 intron variant A/- delins 0.82 4
rs2208589
PREX1
20 48791877 intron variant A/G snv 0.81 1
rs9317097 13 22596235 upstream gene variant C/T snv 0.80 1
rs7794284
GTF2I
7 74683722 intron variant G/A snv 0.80 1
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2969037
LOC107986758
7 2494758 regulatory region variant A/C snv 0.78 1
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs740047
LOC105375397
7 92600848 downstream gene variant C/T snv 0.77 1
rs743507
NOS3
0.882 0.200 7 151010400 intron variant C/T snv 0.77 4