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: rs26232
rs26232
4 0.925 0.160 5 103261019 intron variant C/T snv 0.30 0.830 1.000 2 2010 2019
dbSNP: rs2561477
rs2561477
1 1.000 0.120 5 103273223 intron variant G/A snv 0.24 0.800 1.000 2 2012 2019
dbSNP: rs39984
rs39984
1 1.000 0.120 5 103261591 intron variant G/T snv 0.30 0.800 1.000 1 2012 2012