Gene: LINC01500 ×
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: rs17094983
rs17094983
LINC01500
10 0.776 0.080 14 58722643 intron variant G/A snv 0.12 0.700 1.000 2 2019 2019
dbSNP: rs8020436
rs8020436
LINC01500
10 0.776 0.080 14 58741719 intron variant G/A snv 0.32 0.700 1.000 1 2019 2019