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: rs2296212
rs2296212
5 0.827 0.080 9 2191309 missense variant C/G snv 0.17 0.17 0.010 1.000 1 2013 2013
dbSNP: rs4741651
rs4741651
4 0.851 0.040 9 2194030 downstream gene variant C/T snv 0.24 0.010 1.000 1 2013 2013