Gene: LINC02355 ×
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: rs4835564
rs4835564
LINC02355
1 1.000 0.040 4 149246545 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs6828493
rs6828493
LINC02355
1 1.000 0.040 4 149246261 intron variant C/T snv 0.26 0.700 1.000 1 2017 2017