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: rs1444669684
rs1444669684
36 0.658 0.480 9 21994285 missense variant C/A;T snv 0.020 1.000 2 2011 2018
dbSNP: rs774829510
rs774829510
3 0.882 0.040 9 21971046 missense variant C/A;T snv 0.010 1.000 1 1999 1999