Gene: LINC01602 ×
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: rs1992045
rs1992045
LINC01602 ; LOC105375856
2 8 57928365 intron variant C/T snv 0.14 0.800 1.000 1 2010 2010
dbSNP: rs1992044
rs1992044
LINC01602 ; LOC105375856
2 8 57928349 intron variant G/A;T snv 0.700 1.000 1 2010 2010