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: rs2660
rs2660
4 0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75 0.010 1.000 1 2011 2011
dbSNP: rs34137742
rs34137742
2 0.925 0.080 12 112910856 intron variant C/T snv 0.13 0.010 1.000 1 2011 2011