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: rs6108803
rs6108803
LINC02871
1 20 11014319 intron variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs62185668
rs62185668 		3 0.925 0.120 20 10981287 intron variant C/A snv 0.19 0.010 1.000 1 2016 2016