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: rs1053005
rs1053005
10 0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 0.010 1.000 1 2013 2013
dbSNP: rs17593222
rs17593222
3 0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 0.010 1.000 1 2013 2013
dbSNP: rs2291282
rs2291282
3 0.882 0.120 17 42346547 intron variant T/C snv 1.2E-03 3.4E-04 0.010 1.000 1 2013 2013
dbSNP: rs3816769
rs3816769
4 0.851 0.240 17 42346255 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs744166
rs744166
22 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2015 2015