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: rs1364963022
rs1364963022
4 0.925 0.080 6 151944233 missense variant G/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs200282497
rs200282497
4 0.925 0.080 6 151944239 missense variant G/C snv 3.6E-05 3.5E-05 0.010 1.000 1 2006 2006
dbSNP: rs9397080
rs9397080
2 1.000 0.040 6 152059380 intron variant C/T snv 0.22 0.010 1.000 1 2012 2012