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 0.790 0.900 10 2008 2018
dbSNP: rs578776
rs578776
13 0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 0.050 1.000 5 2009 2014
dbSNP: rs6495308
rs6495308
8 0.851 0.160 15 78615314 intron variant T/C snv 0.29 0.020 1.000 2 2012 2016
dbSNP: rs1317286
rs1317286
6 0.925 0.120 15 78603787 intron variant A/G snv 0.30 0.010 1.000 1 2010 2010
dbSNP: rs147586937
rs147586937
1 1.000 0.080 15 78602096 synonymous variant G/A snv 4.8E-05 2.8E-05 0.010 1.000 1 2011 2011
dbSNP: rs660652
rs660652
3 1.000 0.080 15 78595490 3 prime UTR variant A/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs749747912
rs749747912
1 1.000 0.080 15 78618880 missense variant C/T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs8040868
rs8040868
17 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 0.010 1.000 1 2010 2010