Gene: LINC01358 ×
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: rs1831539
rs1831539
LINC01358
2 1 59094665 intron variant T/C snv 0.41 0.700 1.000 2 2018 2018
dbSNP: rs6668586
rs6668586
LINC01358
1 1 59095695 intron variant G/A;T snv 0.700 1.000 1 2019 2019