Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs151181359
LPAL2
6 160513493 intron variant A/C snv 1.2E-02 1
rs187270959 6 159919224 downstream gene variant A/C snv 6.8E-03 1
rs6938647
LPA
6 160565883 intron variant A/C snv 0.85 1
rs766345636 13 51297734 TF binding site variant A/C snv 3.1E-04 1
rs12664092 6 160527104 downstream gene variant A/C;G snv 1
rs12787909
DSCAML1
11 117675767 intron variant A/G snv 3.6E-02 1
rs1544167
LOC105378084
6 159379992 intron variant A/G snv 0.24 1
rs1620921
LOC105378091
6 160776055 intron variant A/G snv 0.59 1
rs17830011
LOC105378083
6 159011534 intron variant A/G snv 3.4E-02 1
rs62441903
LPA
6 160566028 intron variant A/G snv 9.9E-03 1
rs6927207
PACRG-AS1
6 163319057 intron variant A/G snv 0.56 1
rs754054303
ACAT2
6 159774018 intron variant A/G snv 7.3E-04 1
rs6926458
LPA
1.000 0.040 6 160598834 intron variant A/G;T snv 2
rs3757037 6 161276368 upstream gene variant A/G;T snv 0.44 1
rs41267809
LPA
6 160532610 missense variant A/G;T snv 2.1E-02; 1.2E-05 1
rs6902316
LPAL2
6 160472135 intron variant A/G;T snv 1
rs117026595
LPA
6 160647203 intron variant A/T snv 8.9E-03 1
rs7769089
PRKN
6 161726695 intron variant A/T snv 0.26 1
rs75692336
LPA
6 160609199 intron variant C/A snv 9.2E-02 1
rs41272114
LPA
1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02 2
rs115848955
LPA
6 160610628 intron variant C/A;T snv 1
rs41259144
LPA
6 160601075 missense variant C/A;T snv 1.6E-05; 7.7E-03 1
rs141550222
LPA
6 160570969 intron variant C/G snv 2.1E-02 1
rs294914
FNDC1
6 159208013 intron variant C/G snv 0.11 1
rs4252198
PLG
6 160752696 intron variant C/G snv 1.0E-02 1