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: rs2524079
rs2524079
6 6 31274397 intron variant G/A snv 0.44 0.700 1.000 2 2011 2017
dbSNP: rs116438126
rs116438126
1 6 31348683 intron variant C/T snv 9.0E-03 0.700 1.000 1 2016 2016
dbSNP: rs2249742
rs2249742
7 0.925 0.120 6 31272944 intron variant C/T snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs2524089
rs2524089
3 0.925 0.160 6 31298745 intron variant G/T snv 0.65 0.700 1.000 1 2012 2012