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: rs1539019
rs1539019
6 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.700 1.000 2 2009 2011
dbSNP: rs10157379
rs10157379
3 1 247442297 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12239046
rs12239046
9 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs4925659
rs4925659
3 1 247440161 intron variant G/A snv 0.33 0.700 1.000 1 2011 2011