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: rs775162839
rs775162839
1 1.000 0.040 4 39505705 missense variant C/T snv 4.8E-05 5.6E-05 0.700 1.000 1 2020 2020