Gene: LINC01478 ×
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: rs144171632
rs144171632
LINC01478
1 18 44366700 intron variant G/C snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs17841683
rs17841683
LINC01478
2 18 44504548 intron variant C/G snv 0.10 0.700 1.000 1 2018 2018