Gene: LINC00885 ×
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: rs4927880
rs4927880
LINC00885
1 3 196150687 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9325432
rs9325432
LINC00885
1 3 196147236 intron variant T/C snv 0.23 0.700 1.000 1 2012 2012