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: rs1137101
rs1137101
LEPR
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.060 1.000 6 2007 2019
dbSNP: rs6313
rs6313
HTR2A
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.050 0.800 5 2011 2015
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 1.000 2 2011 2019
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.020 1.000 2 2009 2019
dbSNP: rs1801278
rs1801278
IRS1
38 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 0.020 1.000 2 2006 2016
dbSNP: rs10097555
rs10097555
NRG1
1 1.000 0.080 8 32488779 intron variant G/A snv 0.62 0.010 1.000 1 2015 2015
dbSNP: rs1024610
rs1024610 		3 0.882 0.200 17 34253212 upstream gene variant T/A snv 0.85 0.010 1.000 1 2019 2019
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: rs10433310
rs10433310
MIF-AS1
1 1.000 0.080 22 23896636 intron variant G/A snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs104894578
rs104894578
KCNJ2
6 0.807 0.280 17 70175691 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs1054135
rs1054135
FABP4 ; LOC101927118
5 0.851 0.240 8 81478525 3 prime UTR variant C/T snv 0.17 0.010 1.000 1 2011 2011
dbSNP: rs1056629
rs1056629
MPHOSPH6
6 0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 0.010 1.000 1 2016 2016
dbSNP: rs1063537
rs1063537
ADIPOQ ; ADIPOQ-AS1
6 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs1063856
rs1063856
VWF
14 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs11126184
rs11126184 		2 0.925 0.080 2 68425042 intergenic variant C/A snv 0.55 0.010 1.000 1 2012 2012
dbSNP: rs111942351
rs111942351 		1 1.000 0.080 5 143693985 intron variant A/G snv 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs11211631
rs11211631
TRABD2B
1 1.000 0.080 1 47918069 intron variant A/C snv 0.46 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: rs11588454
rs11588454
LINC02770
1 1.000 0.080 1 191832003 intron variant T/C snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs11610782
rs11610782 		1 1.000 0.080 12 125711743 intergenic variant G/A snv 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs116133558
rs116133558 		1 1.000 0.080 1 203747715 downstream gene variant C/T snv 2.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs116791765
rs116791765 		1 1.000 0.080 11 94347083 intergenic variant T/G snv 2.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs11897825
rs11897825
LOC100507562
1 1.000 0.080 2 21471579 intron variant A/G snv 0.54 0.700 1.000 1 2016 2016
dbSNP: rs12415421
rs12415421
ST8SIA6 ; ST8SIA6-AS1
1 1.000 0.080 10 17391921 intron variant C/T snv 5.4E-02 0.010 1.000 1 2020 2020
dbSNP: rs12518414
rs12518414
GHR
1 1.000 0.080 5 42721976 downstream gene variant G/A snv 0.22 0.010 1.000 1 2018 2018