Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6918289
ADCY10P1
0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02 2
rs7177922
RYR3
0.925 0.040 15 33616418 intron variant G/A snv 0.19 2
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
rs10276782 1.000 0.040 7 24765621 regulatory region variant C/T snv 0.13 1
rs11781551
LOC105375733
1.000 0.040 8 122395852 intergenic variant G/A snv 0.40 1
rs17045031
LOC105377142
1.000 0.040 3 66717940 intergenic variant G/A snv 0.10 1
rs562020
KL
1.000 0.040 13 33017932 intron variant A/G snv 0.69 1
rs567170
KL
1.000 0.040 13 33043649 intron variant C/G snv 0.32 1
rs6601530
PINX1
1.000 0.040 8 10813762 intron variant G/A snv 0.61 1
rs747885829
NLRP3
1.000 0.040 1 247423957 missense variant C/T snv 2.0E-05 1.4E-05 1
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
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