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: rs6065906
rs6065906 		6 20 45925376 downstream gene variant T/A;C;G snv 0.800 1.000 6 2010 2019
dbSNP: rs737337
rs737337
DOCK6
6 0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 0.800 1.000 6 2010 2019
dbSNP: rs103294
rs103294 		7 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 0.800 1.000 5 2012 2019
dbSNP: rs1042034
rs1042034
APOB
15 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 0.800 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: rs13702
rs13702
LPL
7 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.800 1.000 5 2011 2018
dbSNP: rs16942887
rs16942887
PSKH1
2 16 67894139 intron variant G/A snv 0.15 0.800 1.000 5 2010 2019
dbSNP: rs17145738
rs17145738
TBL2
11 0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 0.800 1.000 5 2010 2019
dbSNP: rs17482753
rs17482753 		8 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 0.800 1.000 5 2008 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: rs247617
rs247617 		20 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 0.800 1.000 5 2013 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: rs328
rs328
LPL
19 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.800 1.000 5 2008 2019
dbSNP: rs4660293
rs4660293
PABPC4
5 1 39562508 non coding transcript exon variant A/C;G snv 0.800 1.000 5 2010 2018
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: rs4939883
rs4939883
LOC105372112
5 1.000 0.040 18 49640844 TF binding site variant T/C;G snv 0.800 1.000 5 2009 2019
dbSNP: rs581080
rs581080
TTC39B
3 9 15305380 intron variant G/C snv 0.72 0.800 1.000 5 2010 2019
dbSNP: rs651821
rs651821
APOA5
17 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.800 1.000 5 2012 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: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.800 1.000 4 2011 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