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: rs1260326
rs1260326
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 16 2008 2017
dbSNP: rs964184
rs964184
41 0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83 0.800 13 2009 2017
dbSNP: rs2954029
rs2954029
9 0.846 0.036 8 125478730 intron variant A/T snp 0.43 0.800 9 2009 2017
dbSNP: rs12678919
rs12678919
8 0.923 0.071 8 19986711 intergenic variant A/G snp 9.7E-02 0.800 8 2009 2017
dbSNP: rs780094
rs780094
44 0.699 0.286 2 27518370 intron variant T/C snp 0.67 0.800 8 2007 2017
dbSNP: rs328
rs328
LPL
13 0.821 0.214 8 19962213 stop gained C/G snp 9.2E-02 8.7E-02 0.800 7 2007 2013
dbSNP: rs10401969
rs10401969
20 0.801 0.214 19 19296909 intron variant T/C snp 9.8E-02 0.800 6 2010 2017
dbSNP: rs17145738
rs17145738
7 0.923 0.143 7 73568544 intergenic variant C/T snp 0.11 0.800 6 2008 2017
dbSNP: rs3764261
rs3764261
19 0.769 0.179 16 56959412 intergenic variant C/A snp 0.31 0.800 5 2009 2017
dbSNP: rs439401
rs439401
6 0.878 0.179 19 44911194 non coding transcript exon variant T/C snp 0.68 0.800 5 2009 2012
dbSNP: rs4846914
rs4846914
5 0.923 0.071 1 230159944 intron variant G/A snp 0.45 0.800 5 2008 2017
dbSNP: rs651821
rs651821
10 0.878 0.286 11 116791863 5 prime UTR variant C/T snp 0.88 0.89 0.800 5 2012 2018
dbSNP: rs662799
rs662799
15 0.769 0.321 11 116792991 regulatory region variant G/A snp 0.90 0.800 5 2012 2017
dbSNP: rs10096633
rs10096633
7 1.000 0.036 8 19973410 intergenic variant C/T snp 0.20 0.800 4 2009 2012
dbSNP: rs10503669
rs10503669
6 1.000 0.036 8 19990179 intergenic variant C/A snp 8.2E-02 0.800 4 2008 2017
dbSNP: rs174546
rs174546
10 0.878 0.107 11 61802358 3 prime UTR variant C/T snp 0.30 0.800 4 2009 2017
dbSNP: rs28927680
rs28927680
3 11 116748357 3 prime UTR variant C/G,T snp 9.3E-02 0.800 4 2008 2013
dbSNP: rs4420638
rs4420638
32 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 0.800 4 2007 2017
dbSNP: rs714052
rs714052
3 7 73450539 intron variant A/G snp 9.8E-02 0.800 4 2009 2012
dbSNP: rs1042034
rs1042034
6 2 21002409 missense variant C/T snp 0.70 0.77 0.800 3 2010 2012
dbSNP: rs11613352
rs11613352
4 1.000 0.036 12 57398797 intron variant C/T snp 0.19 0.800 3 2010 2017
dbSNP: rs12721054
rs12721054
2 19 44919330 3 prime UTR variant A/G snp 3.5E-02 0.800 3 2012 2013
dbSNP: rs16996148
rs16996148
6 0.923 0.071 19 19547663 intergenic variant G/T snp 9.5E-02 0.800 3 2008 2012
dbSNP: rs17321515
rs17321515
13 0.784 0.143 8 125474167 intron variant A/G snp 0.50 0.800 3 2008 2012
dbSNP: rs17482753
rs17482753
7 1.000 0.071 8 19975135 intergenic variant G/T snp 8.5E-02 0.800 3 2007 2013