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: rs929641
rs929641
LINC01122
3 2 58565242 intron variant A/G snv 0.45 0.700 1.000 2 2015 2019
dbSNP: rs17049502
rs17049502
LINC01122
1 2 58442749 intron variant A/G snv 0.23 0.700 1.000 1 2019 2019