Gene: LINC01905 ×
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: rs715170
rs715170
LOC642484 ; LINC01539 ; LINC01905
1 1.000 0.040 18 56128283 intron variant C/T snv 0.20 0.700 1.000 3 2015 2019
dbSNP: rs1792709
rs1792709
LOC642484 ; LINC01539 ; LINC01905
1 1.000 0.040 18 56101744 intron variant G/A;T snv 0.21 0.700 1.000 2 2017 2019