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: rs1136201
rs1136201
34 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.100 0.895 38 2000 2018
dbSNP: rs1058808
rs1058808
27 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.040 0.750 4 2013 2017
dbSNP: rs749539903
rs749539903
9 0.827 0.120 17 39726987 missense variant G/A snv 8.4E-06 0.040 1.000 4 2008 2017
dbSNP: rs121913470
rs121913470
13 0.776 0.200 17 39723967 missense variant T/C;G snv 0.030 1.000 3 2017 2019
dbSNP: rs121913471
rs121913471
8 0.807 0.120 17 39724747 missense variant G/A;C;T snv 0.030 1.000 3 2017 2019
dbSNP: rs777081311
rs777081311
3 0.925 0.080 17 39710347 missense variant T/C snv 4.0E-06 0.030 1.000 3 2005 2012
dbSNP: rs1801200
rs1801200
7 0.790 0.200 17 39723335 missense variant A/G;T snv 0.020 1.000 2 2005 2008
dbSNP: rs763193414
rs763193414
7 0.827 0.160 17 39707034 missense variant G/A snv 3.7E-05 4.9E-05 0.020 1.000 2 2016 2018
dbSNP: rs1396809633
rs1396809633
2 0.925 0.080 17 39711979 missense variant A/G snv 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1416532705
rs1416532705
3 0.882 0.080 17 39709435 missense variant C/T snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1485579458
rs1485579458
4 0.851 0.080 17 39723921 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs185670819
rs185670819
2 0.925 0.080 17 39708523 missense variant G/A;C snv 5.0E-04; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs200382130
rs200382130
2 0.925 0.080 17 39710388 missense variant G/T snv 2.0E-04 1.2E-04 0.010 1.000 1 2018 2018
dbSNP: rs2517956
rs2517956
2 0.925 0.080 17 39687606 intron variant G/A snv 0.62 0.010 1.000 1 2015 2015
dbSNP: rs28933368
rs28933368
5 0.851 0.080 17 39725721 missense variant G/A snv 0.010 1.000 1 2014 2014
dbSNP: rs368094521
rs368094521
5 0.925 0.120 17 39724861 missense variant G/A snv 1.2E-03 2.6E-04 0.010 1.000 1 2009 2009
dbSNP: rs747200104
rs747200104
2 0.925 0.080 17 39717388 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs751074421
rs751074421
3 0.925 0.080 17 39715823 missense variant C/T snv 8.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs752295912
rs752295912
6 0.925 0.080 17 39710398 missense variant C/T snv 1.6E-05 0.010 1.000 1 2018 2018
dbSNP: rs757811990
rs757811990
2 0.925 0.080 17 39710413 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs759478535
rs759478535
6 0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs767151455
rs767151455
4 0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs778798172
rs778798172
2 0.925 0.080 17 39723321 missense variant C/T snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs903506
rs903506
2 0.925 0.080 17 39723509 intron variant G/A;T snv 0.61; 4.1E-06 0.010 1.000 1 2010 2010