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: rs121918690
rs121918690
THRB
3 0.882 0.040 3 24127694 missense variant C/T snv 0.010 1.000 1 2016 2016