Gene: LINC00598 ×
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: rs1336486
rs1336486
LINC00548 ; LINC00598
1 13 40210677 intron variant T/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs9603697
rs9603697
LINC00548 ; LINC00598
1 13 40209186 intron variant C/A;T snv 0.700 1.000 1 2019 2019