Gene: LINC01708 ×
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: rs6702619
rs6702619
LINC01708
4 0.851 0.200 1 99580690 intron variant T/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs7543130
rs7543130
LINC01708
2 0.925 0.080 1 99584229 intron variant C/A snv 0.39 0.700 1.000 1 2018 2018