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: rs1906436
rs1906436
3 1.000 0.040 15 53590245 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019