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: rs756465037
rs756465037
LTF
6 0.807 0.200 3 46439392 missense variant C/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2005 2005