Gene: LINC02797 ×
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: rs12129942
rs12129942
LINC02797
1 1.000 0.040 1 72843399 intron variant C/T snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs2422320
rs2422320
LINC02797
1 1.000 0.040 1 72827649 intron variant T/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs2422321
rs2422321
LINC02797
1 1.000 0.040 1 72827710 intron variant A/G snv 0.38 0.700 1.000 1 2016 2016