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: rs2221903
rs2221903
12 0.752 0.360 4 122617757 intron variant C/T snv 0.77 0.010 < 0.001 1 2015 2015
dbSNP: rs907715
rs907715
11 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2015 2015