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: rs1909884
rs1909884
2 0.925 0.120 15 32147097 intron variant G/A snv 0.41 0.010 1.000 1 2006 2006
dbSNP: rs2337980
rs2337980
2 0.925 0.120 15 32151995 intron variant C/T snv 0.45 0.010 1.000 1 2006 2006