Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200483076
SYN3
1.000 0.040 22 32688525 intron variant A/C snv 1
rs8135665
LOC105373027 ; SLC16A8
0.851 0.040 22 38080269 intron variant C/T snv 0.24 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 1
rs1789110 0.925 0.040 18 77147088 regulatory region variant C/A snv 0.63 1
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs8056814
CTRB1
0.925 0.160 16 75218429 upstream gene variant G/A snv 0.16 1
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 4
rs493258
ALDH1A2
0.925 0.040 15 58395681 intron variant T/C snv 0.50 2
rs920915
ALDH1A2
1.000 0.040 15 58396268 intron variant C/G snv 0.55 2
rs1048661
LOXL1-AS1 ; LOXL1
0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 1
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 2
rs8017304
RAD51B
1.000 0.040 14 68318360 intron variant G/A snv 0.54 1
rs9542236
B3GLCT
1.000 0.040 13 31245188 intron variant T/C snv 0.34 1