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: rs12913832
rs12913832
15 0.763 0.200 15 28120472 intron variant A/G snv 0.50 0.800 1.000 4 2010 2013
dbSNP: rs1667394
rs1667394
5 15 28285036 intron variant C/A;T snv 0.800 1.000 4 2007 2018
dbSNP: rs916977
rs916977
5 1.000 0.080 15 28268218 intron variant T/C;G snv 0.800 1.000 2 2008 2013
dbSNP: rs1129038
rs1129038
8 0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 0.700 1.000 1 2013 2013
dbSNP: rs11636232
rs11636232
2 15 28141480 synonymous variant C/T snv 0.25 0.26 0.700 1.000 1 2013 2013
dbSNP: rs12593929
rs12593929
1 15 28114112 intron variant G/A snv 0.78 0.700 1.000 1 2013 2013
dbSNP: rs1635168
rs1635168
3 1.000 0.040 15 28290120 intron variant A/C snv 0.77 0.700 1.000 1 2012 2012
dbSNP: rs16950987
rs16950987
2 15 28281082 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs3935591
rs3935591
1 15 28128866 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs8028689
rs8028689
3 15 28243742 intron variant T/C snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs8039195
rs8039195
3 15 28270938 intron variant C/T snv 0.65 0.700 1.000 1 2012 2012