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: rs2299383
rs2299383
2 1.000 0.080 7 103778399 intron variant C/T snv 0.41 0.700 1.000 1 2018 2018