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: rs1532085
rs1532085
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 6 2009 2013
dbSNP: rs1800775
rs1800775
18 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 5 2008 2013
dbSNP: rs2156552
rs2156552
6 1.000 0.040 18 49655298 downstream gene variant A/G;T snv 0.700 1.000 4 2008 2012
dbSNP: rs7499892
rs7499892
7 16 56972678 intron variant C/G;T snv 0.700 1.000 4 2011 2012
dbSNP: rs13702
rs13702
LPL
7 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.700 1.000 3 2012 2012
dbSNP: rs3890182
rs3890182
5 0.925 0.120 9 104885374 intron variant G/A;T snv 0.700 1.000 3 2008 2012
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: rs711752
rs711752
10 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 3 2008 2013
dbSNP: rs10750097
rs10750097
6 1.000 0.040 11 116793324 upstream gene variant G/A;C snv 0.700 1.000 2 2012 2012
dbSNP: rs11076176
rs11076176
4 16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 0.700 1.000 2 2012 2012
dbSNP: rs13107325
rs13107325
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 2 2010 2013
dbSNP: rs17231506
rs17231506
10 0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 0.700 1.000 2 2012 2012
dbSNP: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 2 2010 2012
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.700 1.000 2 2008 2012
dbSNP: rs2293889
rs2293889
2 8 115586972 intron variant T/C;G snv 2.0E-04; 0.65 0.700 1.000 2 2010 2013
dbSNP: rs2652834
rs2652834
2 15 63104668 intron variant A/C;G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs2925979
rs2925979
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs386000
rs386000
2 19 54288907 intergenic variant C/A;G snv 0.700 1.000 2 2010 2013
dbSNP: rs4660293
rs4660293
5 1 39562508 non coding transcript exon variant A/C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs4846918
rs4846918
3 1 230164840 intron variant C/G;T snv 0.700 1.000 2 2012 2012
dbSNP: rs4939883
rs4939883
5 1.000 0.040 18 49640844 TF binding site variant T/C;G snv 0.700 1.000 2 2009 2009
dbSNP: rs599839
rs599839
27 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 0.700 1.000 2 2012 2013
dbSNP: rs6065906
rs6065906
6 20 45925376 downstream gene variant T/A;C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs673548
rs673548
14 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 2 2012 2012
dbSNP: rs7134594
rs7134594
4 1.000 0.200 12 109562388 intron variant C/G;T snv 0.700 1.000 2 2010 2013