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: rs775921458
rs775921458
1 1.000 0.040 11 17407404 missense variant C/T snv 3.2E-05 4.9E-05 0.010 1.000 1 2018 2018