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 3 2012 2017
dbSNP: rs17061048
rs17061048
LINC00598
2 1.000 0.040 13 40258875 intron variant T/A snv 3.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs915286
rs915286
LINC00598
2 1.000 0.040 13 40121855 intron variant G/A;C snv 0.700 1.000 1 2015 2015