Gene: LINC00598 ×
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: rs941823
rs941823
LINC00598
6 0.827 0.120 13 40439840 intron variant T/C snv 0.77 0.800 1.000 4 2011 2017