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: rs3790844
rs3790844
4 0.882 0.200 1 200038304 intron variant A/C;G snv 0.730 1.000 4 2010 2018
dbSNP: rs3790843
rs3790843
7 0.827 0.160 1 200041696 intron variant C/T snv 0.29 0.020 1.000 2 2015 2018
dbSNP: rs1034925236
rs1034925236
2 0.925 0.120 1 200048258 missense variant G/C snv 0.010 1.000 1 2011 2011