Gene: LINC00513 ×
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: rs205764
rs205764
LINC-PINT ; LINC00513
1 1.000 0.080 7 130913477 intron variant G/T snv 0.65 0.010 1.000 1 2018 2018
dbSNP: rs547311
rs547311
LINC-PINT ; LINC00513
1 1.000 0.080 7 130913695 intron variant G/A snv 0.31 0.010 1.000 1 2018 2018