Gene: LINC00326 ×
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: rs271170
rs271170
LINC00326
2 6 132994665 intron variant T/C snv 0.74 0.700 1.000 1 2013 2013
dbSNP: rs3012465
rs3012465
LINC00326
1 6 133029797 intron variant A/G;T snv 0.700 1.000 1 2014 2014