Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs180749
AGXT2
1.000 0.040 5 35033500 missense variant G/A snv 0.95 0.94 1
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs212528
ECE1
0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs13447720
MRE11
0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs138227502
ADIPOQ-AS1 ; ADIPOQ
0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04 2
rs16881446
HS3ST1
0.925 0.040 4 11406961 intron variant T/C snv 0.27 2
rs4142986
COL15A1
0.925 0.040 9 99052344 intron variant C/A;G;T snv 1.1E-04; 0.75; 4.0E-06 2
rs4552883 0.925 0.040 8 139234730 regulatory region variant G/A;C snv 2
rs499952
MRE11
0.925 0.040 11 94449826 intron variant G/T snv 0.41 2
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
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs569033466
CETP
0.882 0.160 16 56961929 5 prime UTR variant G/A;C;T snv 4.8E-05; 2.4E-05 6
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
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
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
rs4987262
PTGIR
0.882 0.040 19 46623592 missense variant G/A;C snv 7.1E-03 4