Gene: LINC02062 ×
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: rs150992
rs150992
LINC02062
1 5 98939493 intron variant A/G snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs325220
rs325220
LINC02062
1 5 98968860 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019