Gene: LINC01572 ×
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: rs17607347
rs17607347
LINC01572
1 16 72347561 intron variant T/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs62053992
rs62053992
LINC01572
1 16 72355973 intron variant A/C;G snv 0.700 1.000 1 2018 2018