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: rs1917760
rs1917760
1 7 143262206 intron variant G/A;T snv 1.8E-02 0.010 1.000 1 2009 2009
dbSNP: rs5767700
rs5767700
1 22 46216775 intron variant T/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs5767743
rs5767743
1 22 46226097 intron variant T/C snv 0.36 0.010 1.000 1 2015 2015
dbSNP: rs1431648262
rs1431648262
2 8 26756585 3 prime UTR variant G/C snv 1.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs1799904
rs1799904
2 1.000 0.080 5 96429259 missense variant C/A;T snv 4.0E-06; 2.1E-03 0.010 1.000 1 2013 2013
dbSNP: rs771065515
rs771065515
2 1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs3862434
rs3862434
3 1.000 0.080 15 90537155 intron variant A/G snv 0.48 0.010 1.000 1 2014 2014
dbSNP: rs7076156
rs7076156
3 0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 0.010 1.000 1 2014 2014
dbSNP: rs763751076
rs763751076
3 0.925 0.160 2 240875132 missense variant C/T snv 1.2E-05 6.3E-05 0.010 1.000 1 2017 2017
dbSNP: rs11635252
rs11635252
4 0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 0.010 1.000 1 2014 2014
dbSNP: rs150924946
rs150924946
5 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 0.010 1.000 1 2017 2017
dbSNP: rs2331841
rs2331841
5 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 0.010 1.000 1 2019 2019
dbSNP: rs267606841
rs267606841
5 0.882 0.120 2 165749801 missense variant A/C snv 0.010 1.000 1 2014 2014
dbSNP: rs60662302
rs60662302
5 0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 0.010 1.000 1 2017 2017
dbSNP: rs2059806
rs2059806
7 0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 0.020 1.000 2 2015 2017
dbSNP: rs13702
rs13702
LPL
7 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs1572982
rs1572982
HFE
7 0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs301
rs301
LPL
7 0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 0.010 1.000 1 2015 2015
dbSNP: rs553668
rs553668
8 0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs2119882
rs2119882
9 0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 0.010 1.000 1 2019 2019
dbSNP: rs17249754
rs17249754
12 0.882 0.120 12 89666809 intron variant G/A snv 0.15 0.010 1.000 1 2014 2014
dbSNP: rs1800544
rs1800544
12 0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 0.010 1.000 1 2016 2016
dbSNP: rs80356814
rs80356814
15 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs2016520
rs2016520
16 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 0.010 1.000 1 2010 2010
dbSNP: rs182052
rs182052
19 0.701 0.440 3 186842993 intron variant G/A snv 0.38 0.010 1.000 1 2019 2019