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: rs2073764
rs2073764
2 0.925 0.120 22 19811887 intron variant C/T snv 6.0E-03 0.700 1.000 1 2017 2017