Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 3
rs1406961
NKAIN4
20 63264568 intron variant A/C snv 0.87 2
rs2969037
LOC107986758
7 2494758 regulatory region variant A/C snv 0.78 1
rs312053 2 21205177 intergenic variant A/C snv 0.35 1
rs463312
TUBB1
1.000 0.040 20 59022915 missense variant A/C snv 7.7E-02 5.7E-02 1
rs607342 6 139509081 intron variant A/C snv 0.53 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs397509365
LDLR
0.925 0.080 19 11116197 missense variant A/C;G snv 8.0E-06 4
rs7763350 6 43381570 intron variant A/C;G snv 0.44 1
rs9972727 16 31137821 upstream gene variant A/C;G snv 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 4
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 4
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs6770911
MECOM
3 169577976 intron variant A/C;G;T snv 2
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs4975709
IRX4
5 1877166 downstream gene variant A/C;T snv 2
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs6035310
PDYN-AS1
20 2007953 intron variant A/C;T snv 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 12