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: rs116150891
rs116150891
1 1.000 0.040 9 21970929 missense variant G/A;C snv 5.6E-04 2.6E-03 0.700 0
dbSNP: rs6413464
rs6413464
2 1.000 0.040 9 21970980 missense variant C/A;G snv 1.3E-03; 4.1E-06 0.700 0