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: rs2089657
rs2089657
LBH
1 1.000 0.040 2 30247312 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018