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: rs121908668
rs121908668
5 0.882 0.240 11 68357673 missense variant G/T snv 0.010 1.000 1 2003 2003
dbSNP: rs121908673
rs121908673
2 0.925 0.160 11 68363818 missense variant C/T snv 0.010 1.000 1 2005 2005