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: rs1553609210
rs1553609210
THRB
4 0.851 0.040 3 24122984 missense variant C/T snv 0.700 1.000 2 1993 1994