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: rs1024611
rs1024611 		63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs10272006
rs10272006
SP4
3 0.925 0.080 7 21480514 intron variant G/A snv 0.75 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 2019 2019
dbSNP: rs1057156731
rs1057156731
LMNA
3 0.925 0.120 1 156137730 missense variant T/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1057613
rs1057613
MTTP
1 1.000 0.040 4 99583828 3 prime UTR variant G/A snv 0.60 0.010 1.000 1 2014 2014
dbSNP: rs10750097
rs10750097
APOA5
6 1.000 0.040 11 116793324 upstream gene variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs10865710
rs10865710
PPARG
13 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2012 2012
dbSNP: rs10883437
rs10883437 		3 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 0.010 1.000 1 2019 2019
dbSNP: rs11166927
rs11166927
TRAPPC9
1 1.000 0.040 8 139784177 intron variant T/C snv 0.39 0.010 1.000 1 2017 2017
dbSNP: rs11235972
rs11235972
UCP3
1 1.000 0.040 11 74006029 intron variant G/A snv 0.21 0.010 1.000 1 2013 2013
dbSNP: rs1130864
rs1130864
CRP
27 0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 0.010 1.000 1 2018 2018
dbSNP: rs1131580
rs1131580
TNFSF10
4 0.882 0.160 3 172505830 3 prime UTR variant A/C;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1137100
rs1137100
LEPR
39 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 1.000 2 2013 2018
dbSNP: rs1137101
rs1137101
LEPR
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.030 1.000 3 2013 2018
dbSNP: rs11599176
rs11599176
SIRT1
2 0.925 0.080 10 67894017 intron variant A/G snv 0.11 0.010 1.000 1 2018 2018
dbSNP: rs117542855
rs117542855 		1 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs11794552
rs11794552
PLPP7 ; LOC105376299
1 1.000 0.040 9 131344938 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs11820744
rs11820744
OSBPL5 ; LOC107987158
2 1.000 0.040 11 3147308 intron variant C/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs11868035
rs11868035
SREBF1 ; RAI1
14 0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 0.010 1.000 1 2013 2013
dbSNP: rs11932595
rs11932595
CLOCK
12 0.827 0.160 4 55457430 intron variant A/G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs11976006
rs11976006
CREB5
3 1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs12137855
rs12137855
LYPLAL1
3 0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 0.020 1.000 2 2014 2019
dbSNP: rs12152703
rs12152703
KLB
2 0.925 0.120 4 39420199 intron variant G/T snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.050 0.600 5 2007 2016
dbSNP: rs1227756
rs1227756
COL13A1
2 0.925 0.080 10 69828748 intron variant G/A;C snv 0.700 1.000 1 2010 2010