Gene: LINC01505 ×
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: rs9408815
rs9408815
LINC01505
2 9 106128240 intron variant C/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs9409082
rs9409082
LINC01505
2 9 106138768 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs969650
rs969650
LINC01505
1 9 106615799 non coding transcript exon variant T/C snv 0.49 0.700 1.000 1 2019 2019