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: rs1050529
rs1050529
3 0.882 0.040 6 31356838 missense variant C/T snv 0.11 0.700 1.000 1 2016 2016