Source: ALL
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: rs1412239
rs1412239
LINGO2
4 0.925 0.120 9 28425517 intron variant C/G snv 0.26 0.810 1.000 2 2013 2019