Gene: LINC02227 ×
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: rs1952652
rs1952652
LINC02227
3 5 158384080 intron variant A/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs9313772
rs9313772
LINC02227
2 5 158377449 intron variant C/T snv 0.30 0.700 1.000 1 2011 2011