Gene: LINC01122 ×
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: rs2708146
rs2708146
LINC01122
1 1.000 0.120 2 58728818 intron variant A/G snv 0.47 0.710 1.000 2 2019 2019
dbSNP: rs1922786
rs1922786
LINC01122
1 1.000 0.120 2 58636438 intron variant A/G snv 0.29 0.010 1.000 1 2019 2019