Gene: LINC00824 ×
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: rs17804358
rs17804358
LINC00824
1 8 128439451 intron variant C/T snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs4598218
rs4598218
LINC00824
1 8 128471710 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018