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: rs1555650923
rs1555650923
TGIF1
1 1.000 0.120 18 3457389 missense variant C/T snv 0.700 1.000 2 2002 2007