Gene: LINC00595 ×
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: rs1249150
rs1249150
LINC00595
1 10 78220750 intron variant G/A snv 0.77 0.700 1.000 1 2019 2019
dbSNP: rs12767022
rs12767022
LINC00595 ; LOC107984245
1 10 78457709 intron variant G/A snv 8.0E-02 0.700 1.000 1 2019 2019