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: rs2187668
rs2187668
10 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.800 1.000 1 2011 2011
dbSNP: rs4664308
rs4664308
1 0.851 0.160 2 160060986 intron variant A/G snv 0.30 0.800 1.000 1 2011 2011