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: rs11082394
rs11082394
LINC01478
1 18 44491260 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs12606620
rs12606620
LINC01478
1 18 44428132 intron variant G/T snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs12958173
rs12958173
LINC01478
2 18 44562012 intron variant A/C snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs7245273
rs7245273
LINC01478
1 18 44494557 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019