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: rs476141
rs476141
LINC02774
1 1.000 0.120 1 244013122 intron variant G/A;T snv 0.800 1.000 1 2011 2011