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: rs199722402
rs199722402
3 0.925 0.120 15 40987186 missense variant C/T snv 3.1E-04 8.4E-04 0.700 0
dbSNP: rs730882226
rs730882226
3 0.925 0.120 15 41071953 missense variant A/G snv 1.6E-05 4.2E-05 0.700 0