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
7 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.800 0.960 6 2008 2018
dbSNP: rs6495309
rs6495309
3 0.807 0.080 15 78622903 upstream gene variant C/A;T snv 0.740 1.000 3 2008 2014
dbSNP: rs578776
rs578776
3 0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 0.740 1.000 2 2009 2020
dbSNP: rs12914385
rs12914385
8 0.790 0.160 15 78606381 intron variant C/A;T snv 0.730 1.000 2 2009 2012
dbSNP: rs8042374
rs8042374
4 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.710 1.000 3 2008 2012
dbSNP: rs12910984
rs12910984
3 0.827 0.080 15 78599285 intron variant G/A;C;T snv 0.710 1.000 2 2009 2012
dbSNP: rs938682
rs938682
3 0.851 0.080 15 78604205 intron variant G/A snv 0.72 0.710 1.000 2 2009 2016