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: rs4845625
rs4845625
IL6R
9 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.800 1.000 2 2013 2018
dbSNP: rs515135
rs515135 		9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.800 1.000 2 2013 2018
dbSNP: rs590121
rs590121
SERPINH1
1 1.000 0.040 11 75563105 5 prime UTR variant G/T snv 0.36 0.800 1.000 2 2013 2018
dbSNP: rs602633
rs602633 		10 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 0.800 1.000 2 2014 2018
dbSNP: rs6544713
rs6544713
ABCG8
5 0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 0.800 1.000 2 2013 2018
dbSNP: rs6700559
rs6700559
DDX59-AS1
1 1.000 0.040 1 200676945 intron variant C/T snv 0.43 0.800 1.000 2 2013 2018
dbSNP: rs7692387
rs7692387
GUCY1A1
5 0.925 0.080 4 155714157 intron variant G/A snv 0.16 0.800 1.000 2 2013 2018
dbSNP: rs9319428
rs9319428
FLT1
4 0.925 0.080 13 28399484 intron variant G/A snv 0.30 0.800 1.000 2 2013 2018
dbSNP: rs9515203
rs9515203
COL4A2
1 1.000 0.040 13 110397276 intron variant T/C snv 0.26 0.800 1.000 2 2013 2018
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.770 0.875 8 2012 2019
dbSNP: rs9349379
rs9349379
PHACTR1
19 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.760 1.000 11 2015 2019
dbSNP: rs17465637
rs17465637
MIA3
11 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.750 1.000 6 2011 2019
dbSNP: rs2943634
rs2943634 		15 0.763 0.200 2 226203364 intergenic variant A/C;G snv 0.750 1.000 6 2009 2018
dbSNP: rs1746048
rs1746048 		8 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 0.740 1.000 5 2007 2019
dbSNP: rs9818870
rs9818870
MRAS
9 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 0.740 0.600 5 2011 2019
dbSNP: rs11591147
rs11591147
PCSK9
28 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 0.730 1.000 6 2010 2019
dbSNP: rs7412
rs7412
APOE
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.730 1.000 6 2012 2019
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
21 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 0.730 1.000 5 2009 2018
dbSNP: rs12526453
rs12526453
PHACTR1
5 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.730 1.000 4 2013 2019
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.730 1.000 4 2013 2018
dbSNP: rs2107595
rs2107595 		15 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 0.720 1.000 6 2015 2019
dbSNP: rs12190287
rs12190287
TCF21
19 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.720 1.000 4 2013 2017
dbSNP: rs11206510
rs11206510 		16 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 0.720 1.000 3 2010 2015
dbSNP: rs1122608
rs1122608
SMARCA4
16 0.763 0.120 19 11052925 intron variant G/T snv 0.18 0.720 1.000 3 2014 2016
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.720 1.000 3 2009 2015