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: rs121918694
rs121918694
THRB
2 0.925 0.040 3 24143539 missense variant C/G;T snv 0.710 1.000 1 2003 2003