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: rs10106652
rs10106652 		3 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs10184004
rs10184004 		5 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 0.700 1.000 2 2018 2018
dbSNP: rs1041968
rs1041968
APOB
6 2 21009932 synonymous variant G/A snv 0.39 0.38 0.700 1.000 2 2018 2019
dbSNP: rs1045241
rs1045241
TNFAIP8
6 1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 0.700 1.000 2 2018 2018
dbSNP: rs10750097
rs10750097
APOA5
6 1.000 0.040 11 116793324 upstream gene variant G/A;C snv 0.700 1.000 2 2012 2012
dbSNP: rs1077834
rs1077834
LIPC ; ALDH1A2
5 15 58431280 intron variant T/C snv 0.34 0.700 1.000 2 2018 2019
dbSNP: rs10822145
rs10822145
JMJD1C
1 10 63174788 intron variant C/T snv 0.44 0.700 1.000 2 2015 2018
dbSNP: rs10832027
rs10832027
ARNTL
5 11 13335636 intron variant G/A snv 0.67 0.700 1.000 2 2016 2018
dbSNP: rs10861661
rs10861661
RIC8B
1 12 106780868 intron variant A/C snv 0.23 0.700 1.000 2 2017 2017
dbSNP: rs10864728
rs10864728
GALNT2
3 1 230169168 intron variant A/G snv 0.50 0.700 1.000 2 2015 2018
dbSNP: rs10889348
rs10889348
DOCK7
4 1 62612551 intron variant A/T snv 0.32 0.700 1.000 2 2018 2019
dbSNP: rs11207995
rs11207995
DOCK7
4 1 62583880 intron variant A/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs112875651
rs112875651 		7 8 125494452 intron variant G/A snv 0.31 0.700 1.000 2 2018 2019
dbSNP: rs114139997
rs114139997
COL18A1
1 21 45455861 missense variant G/A snv 1.2E-03 5.4E-03 0.700 1.000 2 2014 2018
dbSNP: rs1145198
rs1145198 		2 11 116703620 intergenic variant G/A snv 0.21 0.700 1.000 2 2018 2019
dbSNP: rs115299243
rs115299243
APOE
1 19 44907291 non coding transcript exon variant A/G snv 7.1E-03 0.700 1.000 2 2018 2019
dbSNP: rs11604424
rs11604424
ZPR1
4 11 116780399 intron variant C/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs11967262
rs11967262 		4 6 43792590 intergenic variant C/G snv 0.41 0.700 1.000 2 2019 2019
dbSNP: rs11974409
rs11974409
TBL2
6 0.925 0.120 7 73575060 intron variant A/G snv 0.16 0.700 1.000 2 2009 2012
dbSNP: rs12042319
rs12042319
DOCK7
6 1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 0.700 1.000 2 2016 2019
dbSNP: rs12287066
rs12287066
APOA5
4 11 116791615 synonymous variant G/T snv 7.7E-02 0.10 0.700 1.000 2 2012 2012
dbSNP: rs12423664
rs12423664
FBRSL1
6 1.000 0.040 12 132493308 intron variant G/A snv 0.10 0.700 1.000 2 2018 2018
dbSNP: rs12610185
rs12610185
PBX4
4 19 19610913 intron variant G/A snv 8.6E-02 0.700 1.000 2 2009 2012
dbSNP: rs12679834
rs12679834
LPL
7 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 2 2012 2012
dbSNP: rs13231516
rs13231516
BAZ1B
2 7 73448919 intron variant T/C;G snv 0.700 1.000 2 2016 2019