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: rs2037986
rs2037986
LINC01697
1 1.000 0.080 21 28104158 intron variant G/T snv 0.44 0.700 1.000 1 2007 2007