Gene: LINC02341 ×
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: rs9533090
rs9533090
LINC02341
3 13 42377313 intron variant C/T snv 0.39 0.700 1.000 3 2012 2014
dbSNP: rs8001611
rs8001611
LINC02341
2 13 42391558 intron variant C/T snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs9533095
rs9533095
LINC02341
2 13 42394913 intron variant G/T snv 0.39 0.700 1.000 1 2014 2014