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: rs121909066
rs121909066
TGIF1
1 1.000 0.120 18 3456420 missense variant C/G snv 2.8E-05 4.9E-05 0.800 1.000 2 2000 2004