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: rs780094
rs780094
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.030 1.000 3 2008 2018
dbSNP: rs4363657
rs4363657
5 12 21215788 intron variant T/C snv 0.18 0.020 1.000 2 2015 2019
dbSNP: rs4646188
rs4646188
4 0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 0.020 0.500 2 2018 2018
dbSNP: rs879922
rs879922
4 0.882 0.160 X 15572684 intron variant C/G snv 0.020 1.000 2 2018 2018
dbSNP: rs10488699
rs10488699
1 11 116761784 intron variant C/T snv 1.0E-01 0.010 1.000 1 2017 2017
dbSNP: rs10892151
rs10892151
3 1.000 11 117661016 intron variant C/T snv 9.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs11066782
rs11066782
2 1.000 0.040 12 109472747 intron variant C/T snv 0.17 0.010 1.000 1 2016 2016
dbSNP: rs11613718
rs11613718
2 1.000 0.040 12 109474527 intron variant C/T snv 0.17 0.010 1.000 1 2016 2016
dbSNP: rs12363280
rs12363280
1 11 231980 intron variant C/A;G snv 0.010 1.000 1 2015 2015
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.010 1.000 1 2014 2014
dbSNP: rs1430583
rs1430583
1 4 140565830 intron variant C/T snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs1685354
rs1685354
1 11 74002546 intron variant A/G snv 0.30 0.010 1.000 1 2015 2015
dbSNP: rs174547
rs174547
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2018 2018
dbSNP: rs17465637
rs17465637
11 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs1746661
rs1746661
3 0.925 0.080 1 32869438 intron variant G/A;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs1799884
rs1799884
GCK
6 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.010 1.000 1 2009 2009
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2014 2014
dbSNP: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
dbSNP: rs1978124
rs1978124
2 X 15599940 intron variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs1984112
rs1984112
8 0.807 0.280 7 80613604 intron variant A/G snv 0.33 0.010 1.000 1 2013 2013
dbSNP: rs2070665
rs2070665
2 11 116836968 intron variant A/C;G snv 0.85 0.010 < 0.001 1 2016 2016
dbSNP: rs2070744
rs2070744
54 0.608 0.680 7 150992991 intron variant C/T snv 0.70 0.010 1.000 1 2012 2012
dbSNP: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.010 1.000 1 2014 2014
dbSNP: rs2074192
rs2074192
9 0.827 0.160 X 15564667 intron variant C/T snv 0.40 0.010 1.000 1 2018 2018
dbSNP: rs2075294
rs2075294
1 11 116787406 intron variant G/T snv 3.5E-02 0.010 1.000 1 2019 2019