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: rs587779350
rs587779350
1 1.000 0.120 12 102419619 missense variant G/A snv 7.0E-06 0.700 1.000 1 2014 2014
dbSNP: rs121912430
rs121912430
1 1.000 0.120 12 102419637 missense variant C/T snv 0.700 0
dbSNP: rs121908501
rs121908501
2 0.925 0.240 17 42210189 missense variant C/G snv 0.010 1.000 1 2012 2012