Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs285
LPL
1.000 0.080 8 19957678 intron variant C/T snv 0.59 5
rs35436 1.000 0.080 12 115116718 intergenic variant C/T snv 0.40 5
rs5883
CETP
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 5
rs12130333 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 4
rs463312
TUBB1
1.000 0.040 20 59022915 missense variant A/C snv 7.7E-02 5.7E-02 4
rs1052053
PMF1 ; PMF1-BGLAP
1.000 0.080 1 156232382 missense variant A/C;G snv 1.0E-03; 0.38 3
rs1052700
PLIN1 ; KIF7
1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 3
rs11750568 1.000 0.080 5 179108712 downstream gene variant A/G;T snv 3
rs12204590
LOC112267978 ; LINC01394
1.000 0.080 6 1337158 intergenic variant T/A snv 0.14 3
rs1234442507
TUBB1
1.000 0.040 20 59022915 frameshift variant AG/- del 4.0E-06 3
rs12476527
KCNK3
1.000 0.080 2 26692756 5 prime UTR variant G/C;T snv 3
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs2132572
IGFBP3
1.000 7 45921946 upstream gene variant T/C snv 0.79 3
rs2138533
COL3A1 ; LOC105373791
1.000 0.120 2 188972486 upstream gene variant T/A;C snv 3
rs2219939 1.000 0.040 15 78737381 downstream gene variant G/A snv 0.53 3
rs2238151
ALDH2
1.000 0.040 12 111774029 intron variant T/C snv 0.52 3
rs2301339
CDCA3 ; GNB3
1.000 0.080 12 6845460 3 prime UTR variant G/A;T snv 3
rs42039
CDK6
1.000 0.080 7 92615108 3 prime UTR variant C/T snv 0.19 0.19 3
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 3
rs650439
KL
1.000 0.080 13 33061802 intron variant T/A snv 0.82 0.81 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs7859727
CDKN2B-AS1
1.000 0.080 9 22102166 intron variant C/T snv 0.57 3
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs1003346
TMEM245
1.000 9 109053060 intron variant C/A snv 0.43 2
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2