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
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs783396
CRYBG1
1.000 0.080 6 106539495 missense variant A/C snv 0.93 0.93 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs6544718
ABCG8
0.882 0.120 2 43877786 missense variant T/A;C;G snv 0.84; 4.0E-06 4
rs2468844
SAA2 ; SAA2-SAA4
1.000 0.080 11 18245480 missense variant C/A;T snv 0.84 0.80 1
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1654413
GP6 ; LOC107985325
1.000 0.080 19 55014991 missense variant A/G;T snv 3.7E-05; 2.0E-05; 0.80; 4.4E-04 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4833837
IL21
0.827 0.200 4 122615808 synonymous variant G/A snv 0.74 0.77 5
rs35196866
RXRA ; MIR4669
1.000 0.080 9 134379472 5 prime UTR variant C/A snv 0.74 0.65 1
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs2229383
ILF3
1.000 0.080 19 10683954 synonymous variant G/A;C;T snv 4.0E-06; 0.68 2
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs6565653
SLC26A11
1.000 0.080 17 80227984 intron variant T/A;G snv 4.4E-06; 0.63 1