Gene: LINC02869 ×
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: rs3009947
rs3009947
LINC02869
2 1.000 0.040 1 218515813 intron variant T/C snv 0.47 0.700 1.000 1 2019 2019