Source: ALL
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: rs10042590
rs10042590 		1 5 88477501 intron variant G/A snv 5.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10059884
rs10059884 		5 5 32832368 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1008805
rs1008805
CYP19A1 ; MIR4713HG
7 0.851 0.160 15 51257402 intron variant G/A snv 0.64 0.010 1.000 1 2016 2016
dbSNP: rs1009358
rs1009358
LINC02245 ; LINC02576 ; LOC107984063
2 1.000 0.080 2 65049318 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10107066
rs10107066
DPYSL2
1 8 26542619 intron variant G/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10116277
rs10116277
CDKN2B-AS1
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.010 < 0.001 1 2013 2013
dbSNP: rs1022113606
rs1022113606
SOD3
17 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 0.030 1.000 3 2014 2015
dbSNP: rs10224002
rs10224002
PRKAG2
12 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs10224210
rs10224210
PRKAG2
9 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1030431
rs1030431 		3 8 58399138 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10306135
rs10306135
PTGS1
1 9 122375416 5 prime UTR variant A/T snv 0.14 0.010 1.000 1 2009 2009
dbSNP: rs10409243
rs10409243
DNMT1 ; S1PR2
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1041981
rs1041981
LTA ; LOC100287329
25 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 0.010 1.000 1 2006 2006
dbSNP: rs1042034
rs1042034
APOB
15 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 0.010 1.000 1 2013 2013
dbSNP: rs1042309696
rs1042309696
ACE
2 17 63487006 synonymous variant T/C snv 0.010 1.000 1 2008 2008
dbSNP: rs1042580
rs1042580
THBD
2 20 23046984 3 prime UTR variant T/C snv 0.33 0.010 1.000 1 2007 2007
dbSNP: rs1042713
rs1042713
ADRB2
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 0.500 2 2005 2012
dbSNP: rs1042714
rs1042714
ADRB2
54 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 0.030 0.667 3 2005 2012
dbSNP: rs1044250
rs1044250
ANGPTL4
12 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 0.010 1.000 1 2016 2016
dbSNP: rs1044486
rs1044486
USP36
1 17 78796097 3 prime UTR variant G/A snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs1044498
rs1044498
ENPP1
15 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2011 2011
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.040 1.000 4 2012 2019
dbSNP: rs1047964
rs1047964
BACE1 ; RNF214
3 11 117286177 3 prime UTR variant G/A;C;T snv 0.710 1.000 1 2011 2011
dbSNP: rs1048070
rs1048070
FREM1
1 9 14735055 3 prime UTR variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10500326
rs10500326
UBN1
1 16 4868325 intron variant G/T snv 0.21 0.700 1.000 1 2019 2019