Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs151181359
rs151181359
LPAL2
1 6 160513493 intron variant A/C snv 1.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs187270959
rs187270959 		1 6 159919224 downstream gene variant A/C snv 6.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs6938647
rs6938647
LPA
1 6 160565883 intron variant A/C snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs766345636
rs766345636 		1 13 51297734 TF binding site variant A/C snv 3.1E-04 0.700 1.000 1 2018 2018
dbSNP: rs12664092
rs12664092 		1 6 160527104 downstream gene variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs12787909
rs12787909
DSCAML1
1 11 117675767 intron variant A/G snv 3.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs1544167
rs1544167
LOC105378084
1 6 159379992 intron variant A/G snv 0.24 0.700 1.000 1 2015 2015
dbSNP: rs1620921
rs1620921
LOC105378091
1 6 160776055 intron variant A/G snv 0.59 0.700 1.000 1 2015 2015
dbSNP: rs17830011
rs17830011
LOC105378083
1 6 159011534 intron variant A/G snv 3.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs62441903
rs62441903
LPA
1 6 160566028 intron variant A/G snv 9.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs6927207
rs6927207
PACRG-AS1
1 6 163319057 intron variant A/G snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs754054303
rs754054303
ACAT2
1 6 159774018 intron variant A/G snv 7.3E-04 0.700 1.000 1 2018 2018
dbSNP: rs3757037
rs3757037 		1 6 161276368 upstream gene variant A/G;T snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs41267809
rs41267809
LPA
1 6 160532610 missense variant A/G;T snv 2.1E-02; 1.2E-05 0.700 1.000 1 2017 2017
dbSNP: rs6902316
rs6902316
LPAL2
1 6 160472135 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6926458
rs6926458
LPA
2 1.000 0.040 6 160598834 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs117026595
rs117026595
LPA
1 6 160647203 intron variant A/T snv 8.9E-03 0.700 1.000 1 2017 2017
dbSNP: rs7769089
rs7769089
PRKN
1 6 161726695 intron variant A/T snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs75692336
rs75692336
LPA
1 6 160609199 intron variant C/A snv 9.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs115848955
rs115848955
LPA
1 6 160610628 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs41259144
rs41259144
LPA
1 6 160601075 missense variant C/A;T snv 1.6E-05; 7.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs41272114
rs41272114
LPA
2 1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs141550222
rs141550222
LPA
1 6 160570969 intron variant C/G snv 2.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs294914
rs294914
FNDC1
1 6 159208013 intron variant C/G snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs4252198
rs4252198
PLG
1 6 160752696 intron variant C/G snv 1.0E-02 0.700 1.000 1 2017 2017