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: rs116843064
rs116843064
ANGPTL4
16 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 0.700 1.000 7 2014 2019
dbSNP: rs1077835
rs1077835
LIPC ; ALDH1A2
5 15 58431227 intron variant A/G snv 0.34 0.700 1.000 5 2015 2019
dbSNP: rs2954021
rs2954021 		15 1.000 0.040 8 125469835 intron variant A/G snv 0.54 0.700 1.000 5 2017 2019
dbSNP: rs58542926
rs58542926
TM6SF2
42 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 0.700 1.000 5 2015 2019
dbSNP: rs7350481
rs7350481 		8 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 0.700 1.000 5 2010 2019
dbSNP: rs115849089
rs115849089 		7 8 20054859 intergenic variant G/A snv 9.8E-02 0.700 1.000 4 2015 2019
dbSNP: rs174551
rs174551
FADS1 ; FADS2
6 11 61806212 5 prime UTR variant T/C snv 0.28 0.700 1.000 4 2018 2019
dbSNP: rs2954022
rs2954022 		4 8 125470379 intron variant C/A;T snv 0.700 1.000 4 2017 2019
dbSNP: rs508487
rs508487
TAGLN ; PCSK7
4 11 117204850 3 prime UTR variant C/T snv 5.2E-02 0.700 1.000 4 2011 2019
dbSNP: rs55707100
rs55707100
MAP1A
3 15 43528519 missense variant C/T snv 2.2E-02 2.0E-02 0.700 1.000 4 2014 2019
dbSNP: rs13108218
rs13108218
HGFAC
7 4 3442204 intron variant A/G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs138570705
rs138570705
FRMD5
2 15 43974532 intron variant G/A snv 2.0E-02 0.700 1.000 3 2015 2019
dbSNP: rs1495743
rs1495743 		6 8 18415790 intergenic variant G/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs150844304
rs150844304
TP53BP1
4 15 43434427 intron variant A/C;G snv 0.700 1.000 3 2016 2019
dbSNP: rs157582
rs157582
TOMM40
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.700 1.000 3 2016 2019
dbSNP: rs174529
rs174529
MYRF ; TMEM258
7 11 61776489 intron variant T/C snv 0.34 0.700 1.000 3 2015 2019
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
15 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 0.700 1.000 3 2018 2019
dbSNP: rs264
rs264
LPL
6 0.882 0.080 8 19955669 intron variant G/A snv 0.14 0.700 1.000 3 2009 2013
dbSNP: rs2925979
rs2925979
CMIP
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs41274050
rs41274050
A1CF ; ASAH2B
4 10 50814012 missense variant C/A;T snv 4.0E-06; 5.3E-03 0.700 1.000 3 2017 2019
dbSNP: rs4665710
rs4665710 		6 2 20998163 downstream gene variant A/C snv 0.76 0.700 1.000 3 2015 2019
dbSNP: rs769455
rs769455
APOE
8 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 0.700 1.000 3 2014 2019
dbSNP: rs8102280
rs8102280
MAU2
3 19 19344941 non coding transcript exon variant G/A snv 2.8E-02 1.5E-02 0.700 1.000 3 2016 2019
dbSNP: rs9638182
rs9638182 		3 7 73584775 intergenic variant T/G snv 0.16 0.700 1.000 3 2015 2019
dbSNP: rs9988450
rs9988450
DOCK7
3 1 62458777 non coding transcript exon variant C/T snv 0.39 0.700 1.000 3 2015 2019