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: rs1084651
rs1084651
2 6 160668785 intron variant G/A snv 0.23 0.700 1.000 2 2010 2012
dbSNP: rs1689800
rs1689800
2 1 182199750 intron variant A/G snv 0.34 0.700 1.000 2 2010 2013
dbSNP: rs16942887
rs16942887
2 16 67894139 intron variant G/A snv 0.15 0.700 1.000 2 2010 2013
dbSNP: rs2107369
rs2107369
2 16 68082115 intron variant T/G snv 0.18 0.700 1.000 2 2012 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: rs2923084
rs2923084
2 11 10367235 intron variant A/G snv 0.29 0.700 1.000 2 2010 2013
dbSNP: rs3136441
rs3136441
F2
2 11 46721697 intron variant T/C snv 0.13 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: rs4148008
rs4148008
2 17 68879153 non coding transcript exon variant C/G snv 0.40 0.700 1.000 2 2010 2013
dbSNP: rs7255436
rs7255436
2 19 8368312 intron variant C/A snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs10099160
rs10099160
LPL
2 8 19964304 intron variant T/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs10120087
rs10120087
2 9 104898869 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10149080
rs10149080
2 14 54889676 intron variant C/T snv 4.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10200587
rs10200587
2 2 202554561 intron variant A/G snv 7.0E-03 0.700 1.000 1 2012 2012
dbSNP: rs10212938
rs10212938
2 4 155207180 non coding transcript exon variant T/C snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10239940
rs10239940
2 7 73487060 intron variant A/T snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10305650
rs10305650
2 1 150876501 intron variant G/A;C snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs10305685
rs10305685
2 1 150838529 intron variant T/C snv 5.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10405178
rs10405178
2 19 19064943 intron variant T/G snv 2.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs10411413
rs10411413
2 19 19009572 intron variant C/T snv 2.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10422058
rs10422058
2 19 19047391 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10427943
rs10427943
2 22 24131331 intron variant G/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10501321
rs10501321
2 11 47273075 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs10773105
rs10773105
2 12 124799220 intron variant C/T snv 0.63 0.700 1.000 1 2012 2012