Gene: LINC00886 ×
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: rs9859058
rs9859058
LINC00886
2 1.000 0.040 3 156795028 intron variant C/A snv 0.39 0.700 1.000 1 2019 2019