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: rs174547
rs174547
21 0.846 0.071 11 61803311 intron variant T/C snp 0.30 0.800 2 2012 2016
dbSNP: rs6065904
rs6065904
4 20 45906012 intron variant G/A snp 0.23 0.800 2 2009 2012
dbSNP: rs11075253
rs11075253
1 16 15054789 intron variant C/A snp 0.21 0.800 1 2012 2012
dbSNP: rs115136538
rs115136538
1 4 72456848 intron variant T/C snp 7.4E-03 0.800 1 2012 2012
dbSNP: rs115849089
rs115849089
7 8 20054859 regulatory region variant G/A snp 9.4E-02 0.800 1 2012 2012
dbSNP: rs1168029
rs1168029
1 1 62503731 intron variant G/A,C snp 0.58 0.800 1 2012 2012
dbSNP: rs13247874
rs13247874
1 7 73596112 intron variant C/T snp 0.15 0.15 0.800 1 2012 2012
dbSNP: rs2229738
rs2229738
2 11 68794860 missense variant C/G,T snp 6.3E-02 7.1E-02 0.800 1 2012 2012
dbSNP: rs2575876
rs2575876
4 9 104903458 intron variant G/A snp 0.22 0.800 1 2012 2012
dbSNP: rs35853021
rs35853021
1 15 58388444 intron variant G/T snp 0.39 0.800 1 2012 2012
dbSNP: rs3764261
rs3764261
19 0.769 0.179 16 56959412 intergenic variant C/A snp 0.31 0.800 1 2012 2012
dbSNP: rs55791371
rs55791371
3 0.923 0.036 19 11077477 A/C snp 0.10 0.800 1 2012 2012
dbSNP: rs651821
rs651821
10 0.878 0.286 11 116791863 5 prime UTR variant C/T snp 0.88 0.89 0.800 1 2012 2012
dbSNP: rs67418890
rs67418890
1 1 161571067 intron variant T/A,C snp 9.5E-02; 6.9E-05 0.800 1 2012 2012
dbSNP: rs6917603
rs6917603
1 6 30049294 intron variant T/C snp 0.14 0.800 1 2012 2012
dbSNP: rs7228085
rs7228085
1 18 49634444 intergenic variant A/G snp 0.54 0.800 1 2012 2012
dbSNP: rs72669744
rs72669744
1 1 55650832 intron variant C/T snp 2.6E-02 0.800 1 2012 2012
dbSNP: rs7412
rs7412
40 0.642 0.357 19 44908822 missense variant C/T snp 6.2E-02 8.3E-02 0.800 1 2012 2012
dbSNP: rs1059611
rs1059611
LPL
3 8 19967052 3 prime UTR variant T/C snp 0.12 0.700 1 2009 2009
dbSNP: rs10889353
rs10889353
4 1 62652525 intron variant A/C,T snp 0.33 0.700 1 2009 2009
dbSNP: rs1160985
rs1160985
5 1.000 0.071 19 44900155 intron variant C/T snp 0.51 0.700 1 2013 2013
dbSNP: rs11644601
rs11644601
2 16 15078261 intron variant T/C snp 0.19 0.700 1 2016 2016
dbSNP: rs1167998
rs1167998
5 1 62465961 intron variant C/A snp 0.58 0.700 1 2009 2009
dbSNP: rs1168041
rs1168041
2 1 62494579 non coding transcript exon variant T/C snp 0.62 0.700 1 2016 2016
dbSNP: rs1260326
rs1260326
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2009 2009