Gene: LINC01122 ×
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: rs10865309
rs10865309
LINC01122
1 2 58757735 intron variant C/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs77732866
rs77732866
LINC01122
1 2 58752744 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019