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: rs6494537
rs6494537
2 15 65759007 intron variant C/G;T snv 0.800 1.000 2 2010 2012
dbSNP: rs2572207
rs2572207
3 15 65778355 intron variant C/A;T snv 0.700 1.000 2 2016 2017
dbSNP: rs11857609
rs11857609
3 15 65802932 intron variant T/C snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs28498859
rs28498859
2 15 65775439 intron variant A/G snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs7181649
rs7181649
1 15 65762011 intron variant T/C snv 0.37 0.700 1.000 1 2016 2016