Gene: LINC01592 ×
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: rs2912522
rs2912522
LINC01592
2 0.925 0.120 8 69080145 intron variant G/A snv 0.73 0.700 1.000 2 2011 2017
dbSNP: rs629535
rs629535
LINC01592
1 1.000 0.120 8 69095703 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017