Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs868014
MTHFR ; C1orf167
1.000 0.080 1 11789390 missense variant A/G snv 0.99 0.94 1
rs783396
CRYBG1
1.000 0.080 6 106539495 missense variant A/C snv 0.93 0.93 2
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
rs1492099
AGTR1
0.882 0.120 3 148719716 intron variant T/A;C snv 0.89 5
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs1934066
KIF26B
1.000 0.080 1 245508389 intron variant C/T snv 0.85 1
rs2666433
MIR34AHG ; MIR34A
0.925 0.080 1 9153118 intron variant A/G snv 0.82 2
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs2468844
SAA2 ; SAA2-SAA4
1.000 0.080 11 18245480 missense variant C/A;T snv 0.84 0.80 1
rs7620580
KALRN
1.000 0.080 3 124326456 intron variant G/A snv 0.80 1
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4962153
ADAMTS13 ; CACFD1
0.925 0.120 9 133458632 intron variant A/G snv 0.79 9
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10204475
UBR3
1.000 0.080 2 170076012 intron variant T/G snv 0.78 1
rs1864169
GTF2A1 ; SNORA79
0.851 0.200 14 81203689 intron variant G/T snv 0.78 5
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs4833837
IL21
0.827 0.200 4 122615808 synonymous variant G/A snv 0.74 0.77 5
rs2740483
ABCA1 ; LOC105376196
0.882 0.120 9 104928254 intron variant G/C snv 0.75 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs9526212
LRCH1
1.000 0.080 13 46651610 intron variant A/G snv 0.74 2