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: rs2904880
rs2904880
5 1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 0.700 1.000 1 2013 2013