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: rs12942547
rs12942547
7 0.807 0.200 17 42375526 intron variant A/G;T snv 0.700 1.000 3 2015 2017
dbSNP: rs744166
rs744166
22 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.030 1.000 3 2012 2014
dbSNP: rs2293152
rs2293152
10 0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 0.020 1.000 2 2014 2016
dbSNP: rs113994136
rs113994136
7 0.827 0.240 17 42329642 missense variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs3816769
rs3816769
4 0.851 0.240 17 42346255 intron variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs4796793
rs4796793
16 0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 0.010 < 0.001 1 2014 2014
dbSNP: rs8074524
rs8074524
2 0.925 0.040 17 42317580 intron variant C/T snv 0.25 0.010 1.000 1 2016 2016