Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1059611
LPL
8 19967052 3 prime UTR variant T/C snv 0.13 3
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 5
rs11075253
PDXDC1 ; NTAN1
16 15054789 intron variant C/A snv 0.22 1
rs115136538
ADAMTS3
4 72456848 intron variant T/C snv 5.7E-03 1
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs11644601
RRN3 ; PDXDC1
16 15078261 intron variant T/C snv 0.21 4
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs1168029
DOCK7
1 62503731 intron variant G/A;C snv 1
rs1168041
DOCK7
1 62494579 non coding transcript exon variant T/C snv 0.61 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 4
rs13247874
MLXIPL
7 73596112 intron variant C/T snv 0.15 0.15 1
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs17111684
USP24
1 55159875 intron variant C/T snv 3.8E-02 4
rs17249141
LDLR
19 11089332 upstream gene variant C/T snv 3.3E-03 4
rs17267292
GPC5 ; LOC105370315
13 92670893 intron variant T/C snv 0.22 2
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs17610395
CPT1A
11 68794860 missense variant C/G;T snv 1
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs181807530
MINK1
17 4871519 intron variant C/G snv 4.8E-03 1
rs186183604
RAD9A ; LOC100130987
11 67361262 intron variant G/A;T snv 1
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10