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: rs2925979
rs2925979
CMIP
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.800 1.000 9 2010 2019
dbSNP: rs2156552
rs2156552
LOC105372112
6 1.000 0.040 18 49655298 downstream gene variant A/G;T snv 0.800 1.000 7 2008 2019
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.800 1.000 7 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: 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: rs261291
rs261291
ALDH1A2
5 1.000 0.080 15 58387979 intron variant T/A;C snv 0.700 1.000 5 2015 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: 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: 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: rs12748152
rs12748152 		8 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 0.800 1.000 4 2013 2018
dbSNP: rs247616
rs247616 		8 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 0.700 1.000 4 2010 2019
dbSNP: rs5167
rs5167
APOC2 ; APOC4 ; APOC4-APOC2
7 1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 0.800 1.000 4 2012 2019
dbSNP: rs5883
rs5883
CETP
5 1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 0.800 1.000 4 2012 2019
dbSNP: rs711752
rs711752
CETP
10 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.800 1.000 4 2008 2016
dbSNP: rs12801636
rs12801636
PCNX3
5 1.000 0.040 11 65623846 intron variant G/A snv 0.25 0.800 1.000 3 2013 2018
dbSNP: rs15285
rs15285
LPL
5 1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 0.700 1.000 3 2017 2019
dbSNP: rs16940212
rs16940212
ALDH1A2
4 1.000 0.040 15 58401821 intron variant G/A;T snv 0.800 1.000 3 2011 2019
dbSNP: rs17410962
rs17410962 		7 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 0.800 1.000 3 2012 2019
dbSNP: rs17489282
rs17489282 		5 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 0.800 1.000 3 2012 2019
dbSNP: rs2126259
rs2126259
LOC157273
9 1.000 8 9327636 intron variant T/C snv 0.87 0.800 1.000 3 2013 2019
dbSNP: rs2271293
rs2271293
NUTF2
3 1.000 0.040 16 67868167 intron variant G/A snv 0.11 0.800 1.000 3 2009 2019
dbSNP: rs2278426
rs2278426
ANGPTL8 ; DOCK6
11 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 0.800 1.000 3 2013 2019
dbSNP: rs2338104
rs2338104
KCTD10
3 1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 0.800 1.000 3 2008 2019