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: rs121908356
rs121908356
2 0.925 0.120 11 67490804 stop gained C/A snv 0.010 1.000 1 2007 2007
dbSNP: rs121913377
rs121913377
480 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.010 1.000 1 2016 2016
dbSNP: rs1290398674
rs1290398674
5 0.851 0.240 20 58854075 missense variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs267606541
rs267606541
AIP
5 0.827 0.160 11 67487147 stop gained C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs2854744
rs2854744
20 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2018 2018
dbSNP: rs775888932
rs775888932
1 1.000 0.120 2 96115223 missense variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2018 2018
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2011 2017
dbSNP: rs113488022
rs113488022
490 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs760330563
rs760330563
1 1.000 0.120 8 30180515 missense variant C/T snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs104894195
rs104894195
AIP
4 0.882 0.120 11 67490910 stop gained C/G;T snv 4.0E-06; 1.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs763751076
rs763751076
3 0.925 0.160 2 240875132 missense variant C/T snv 1.2E-05 6.3E-05 0.010 1.000 1 2017 2017
dbSNP: rs142833529
rs142833529
1 1.000 0.120 12 12718195 missense variant T/A;C;G snv 1.2E-05; 5.3E-04 0.010 1.000 1 2012 2012
dbSNP: rs765502229
rs765502229
1 1.000 0.120 14 94116511 missense variant T/C snv 1.6E-05 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs77375493
rs77375493
187 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 0.010 1.000 1 2012 2012
dbSNP: rs73637412
rs73637412
4 0.882 0.160 X 137030751 missense variant C/G;T snv 3.5E-03; 1.5E-03 0.050 1.000 5 2014 2019
dbSNP: rs2276020
rs2276020
2 1.000 0.120 11 67490085 missense variant C/G;T snv 3.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs34037914
rs34037914
1 1.000 0.120 16 1079501 synonymous variant C/T snv 5.9E-02 4.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs2066853
rs2066853
AHR
34 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.020 1.000 2 2014 2019
dbSNP: rs1052133
rs1052133
147 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 < 0.001 1 2013 2013
dbSNP: rs5498
rs5498
99 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 < 0.001 1 2015 2015
dbSNP: rs169068
rs169068
12 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 0.010 1.000 1 2011 2011
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2017
dbSNP: rs642249
rs642249
1 1.000 0.120 16 1079912 synonymous variant A/G snv 0.96 0.96 0.010 1.000 1 2011 2011