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: rs1051730
rs1051730
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.100 0.947 19 2008 2018
dbSNP: rs578776
rs578776
13 0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 0.040 1.000 4 2010 2020
dbSNP: rs6495309
rs6495309
10 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 0.040 1.000 4 2009 2014
dbSNP: rs12914385
rs12914385
18 0.790 0.160 15 78606381 intron variant C/A;T snv 0.030 1.000 3 2010 2012
dbSNP: rs3743073
rs3743073
11 0.807 0.120 15 78617197 intron variant G/T snv 0.61 0.030 0.667 3 2010 2013
dbSNP: rs11637630
rs11637630
6 0.882 0.080 15 78607377 intron variant G/A snv 0.71 0.010 1.000 1 2015 2015
dbSNP: rs12910984
rs12910984
8 0.827 0.080 15 78599285 intron variant G/A;C;T snv 0.010 1.000 1 2009 2009
dbSNP: rs2869546
rs2869546
5 0.851 0.120 15 78615003 intron variant C/T snv 0.64 0.010 1.000 1 2015 2015
dbSNP: rs3743078
rs3743078
7 0.807 0.160 15 78602417 intron variant C/A;G snv 0.010 1.000 1 2010 2010
dbSNP: rs6495308
rs6495308
8 0.851 0.160 15 78615314 intron variant T/C snv 0.29 0.010 1.000 1 2016 2016
dbSNP: rs7177514
rs7177514
6 0.882 0.080 15 78615064 intron variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs8040868
rs8040868
17 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 0.010 1.000 1 2018 2018
dbSNP: rs8042059
rs8042059
6 0.882 0.080 15 78615517 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs8042374
rs8042374
10 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.010 1.000 1 2011 2011
dbSNP: rs938682
rs938682
7 0.851 0.080 15 78604205 intron variant G/A snv 0.72 0.010 1.000 1 2016 2016