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: rs1883025
rs1883025
ABCA1
13 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 12 2009 2019
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.800 1.000 10 2009 2019
dbSNP: rs2925979
rs2925979
CMIP
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.800 1.000 9 2010 2019
dbSNP: rs4846914
rs4846914
GALNT2
6 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.800 1.000 9 2008 2019
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.800 1.000 7 2012 2019
dbSNP: rs7499892
rs7499892
CETP
7 16 56972678 intron variant C/G;T snv 0.800 1.000 7 2011 2019
dbSNP: rs10468017
rs10468017
ALDH1A2
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 6 2009 2019
dbSNP: rs1532624
rs1532624
CETP
12 0.851 0.160 16 56971567 intron variant C/A snv 0.34 0.800 1.000 6 2009 2019
dbSNP: rs2954029
rs2954029 		14 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 6 2010 2019
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
5 15 58431280 intron variant T/C snv 0.34 0.700 1.000 5 2010 2019
dbSNP: rs12686004
rs12686004
ABCA1
6 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 0.800 1.000 5 2011 2019
dbSNP: rs16942887
rs16942887
PSKH1
2 16 67894139 intron variant G/A snv 0.15 0.800 1.000 5 2010 2019
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 5 2008 2019
dbSNP: rs1864163
rs1864163
CETP
10 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.800 1.000 5 2008 2019
dbSNP: rs2144300
rs2144300
GALNT2
7 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.800 1.000 5 2008 2018
dbSNP: rs261291
rs261291
ALDH1A2
5 1.000 0.080 15 58387979 intron variant T/A;C snv 0.700 1.000 5 2015 2019
dbSNP: rs261334
rs261334
LIPC ; ALDH1A2 ; LIPC-AS1
5 15 58434545 intron variant G/C snv 0.73 0.800 1.000 5 2010 2019
dbSNP: rs2678379
rs2678379
APOB
8 1.000 0.080 2 21003688 intron variant A/G snv 0.76 0.800 1.000 5 2012 2019
dbSNP: rs2740488
rs2740488
ABCA1
9 0.827 0.120 9 104899461 intron variant A/C snv 0.29 0.700 1.000 5 2015 2019
dbSNP: rs4759375
rs4759375
SBNO1
3 12 123311691 intron variant C/T snv 7.8E-02 0.800 1.000 5 2010 2019
dbSNP: rs4775041
rs4775041
ALDH1A2
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 5 2008 2019
dbSNP: rs581080
rs581080
TTC39B
3 9 15305380 intron variant G/C snv 0.72 0.800 1.000 5 2010 2019
dbSNP: rs7134594
rs7134594
MMAB
4 1.000 0.200 12 109562388 intron variant C/G;T snv 0.800 1.000 5 2010 2019
dbSNP: rs11613352
rs11613352
R3HDM2
9 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.800 1.000 4 2010 2018
dbSNP: rs11869286
rs11869286
STARD3
4 0.925 0.080 17 39657603 intron variant G/C snv 0.52 0.800 1.000 4 2010 2019