Gene: LINC02661 ×
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: rs7906104
rs7906104
LINC02661
3 1.000 0.080 10 108737343 intron variant C/T snv 0.29 0.700 1.000 1 2019 2019