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: rs1032466
rs1032466
1 1.000 0.120 14 50607743 intron variant A/C snv 0.27 0.700 1.000 1 2017 2017