Gene: LINC01091 ×
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: rs7692299
rs7692299
LINC01091
2 0.925 0.120 4 123789429 intron variant C/T snv 0.15 0.700 1.000 1 2017 2017