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: rs2059865
rs2059865
2 1.000 0.040 5 31766326 intron variant T/A snv 0.20 0.700 1.000 1 2014 2014