Gene: LINC00877 ×
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: rs10587701
rs10587701
LINC00877
1 3 72238120 intron variant CT/- delins 0.700 1.000 1 2016 2016
dbSNP: rs4282028
rs4282028
LINC00877
1 3 72240019 intron variant T/C snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs7432379
rs7432379
LINC00877
1 3 72237750 intron variant T/A;C snv 0.60 0.700 1.000 1 2016 2016