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: rs1551570
rs1551570
2 0.925 0.080 19 10107354 intron variant C/T snv 0.59 0.800 1.000 1 2013 2013
dbSNP: rs2305795
rs2305795
2 0.925 0.080 19 10115376 intron variant G/A;C snv 0.010 1.000 1 2011 2011