Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs749582333
NOX4
0.925 0.040 11 89340157 frameshift variant G/- delins 2
rs750996166
USF1
0.925 0.040 1 161041409 stop gained G/A snv 4.0E-06 7.0E-06 2
rs767523236
MPO
0.925 0.040 17 58279033 missense variant T/C snv 4.1E-06 7.0E-06 2
rs769442590
LPL
0.925 0.040 8 19960927 missense variant A/C;G snv 1.6E-05 2
rs915014
C1orf167 ; MTHFR
0.925 0.040 1 11789412 missense variant T/C snv 2
rs180749
AGXT2
1.000 0.040 5 35033500 missense variant G/A snv 0.95 0.94 1
rs1866389
THBS4
0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs2229116
RYR3
0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6
rs7439293
PALLD
0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs121918313
LRP6 ; BCL2L14
0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 4
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1298417395
COP1
0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs4845617
IL6R-AS1 ; IL6R
0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs755460305
KNG1
0.882 0.080 3 186732650 missense variant C/A snv 4