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: rs116843064
rs116843064
16 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 0.700 1.000 7 2014 2019
dbSNP: rs4841132
rs4841132
14 8 9326086 non coding transcript exon variant A/G snv 0.89 0.700 1.000 6 2015 2019
dbSNP: rs1077834
rs1077834
5 15 58431280 intron variant T/C snv 0.34 0.700 1.000 5 2010 2019
dbSNP: rs261291
rs261291
5 1.000 0.080 15 58387979 intron variant T/A;C snv 0.700 1.000 5 2015 2019
dbSNP: rs2740488
rs2740488
9 0.827 0.120 9 104899461 intron variant A/C snv 0.29 0.700 1.000 5 2015 2019
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: rs429358
rs429358
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 4 2015 2018
dbSNP: rs7412
rs7412
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 4 2017 2019
dbSNP: rs115849089
rs115849089
7 8 20054859 intergenic variant G/A snv 9.8E-02 0.700 1.000 3 2015 2019
dbSNP: rs13135092
rs13135092
4 4 102276925 intron variant A/G snv 5.1E-02 0.700 1.000 3 2015 2019
dbSNP: rs13241165
rs13241165
2 7 130747779 intergenic variant A/T snv 0.40 0.700 1.000 3 2015 2019
dbSNP: rs13329672
rs13329672
4 15 58407738 intron variant C/T snv 0.31 0.700 1.000 3 2018 2019
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: rs2075291
rs2075291
15 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 0.700 1.000 3 2018 2019
dbSNP: rs2241208
rs2241208
2 12 109524990 intron variant G/C snv 0.57 0.700 1.000 3 2015 2019
dbSNP: rs2255141
rs2255141
5 10 112174128 intron variant A/G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs235314
rs235314
3 21 44851537 missense variant C/T snv 0.48 0.46 0.700 1.000 3 2018 2019
dbSNP: rs2472386
rs2472386
3 1.000 0.040 9 104839260 intron variant G/A snv 0.47 0.700 1.000 3 2016 2019
dbSNP: rs2642438
rs2642438
6 1 220796686 missense variant A/G snv 0.75 0.78 0.700 1.000 3 2018 2019
dbSNP: rs28526159
rs28526159
2 8 20033716 regulatory region variant C/T snv 0.73 0.700 1.000 3 2016 2019
dbSNP: rs2954022
rs2954022
4 8 125470379 intron variant C/A;T snv 0.700 1.000 3 2015 2019
dbSNP: rs4871137
rs4871137
2 8 120856311 intergenic variant G/T snv 0.55 0.700 1.000 3 2016 2017
dbSNP: rs56156922
rs56156922
5 16 56953457 intergenic variant T/C snv 0.26 0.700 1.000 3 2018 2019
dbSNP: rs5882
rs5882
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.700 1.000 3 2008 2012
dbSNP: rs6601299
rs6601299
5 0.925 0.040 8 9327181 intron variant T/C snv 0.88 0.700 1.000 3 2011 2019