Gene: LINC02657 ×
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: rs7099771
rs7099771
LINC02657
1 10 5612779 intron variant A/G snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs7907173
rs7907173
LINC02657
1 10 5606824 intron variant G/A snv 0.38 0.700 1.000 1 2019 2019