Disease: Cardiovascular Diseases
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
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
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs113230003
PGPEP1
19 18350146 intron variant G/A snv 0.25 2
rs1845034 6 50335316 intergenic variant C/T snv 0.22 2
rs2613498
LOC105378797
1 72287256 intron variant C/T snv 0.20 2
rs7694531
UNC5C
4 95165950 3 prime UTR variant A/G snv 0.64 2
rs943346
SORBS1
10 95494548 intron variant C/G;T snv 2