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: rs121918695
rs121918695
THRB
3 0.882 0.080 3 24127696 missense variant C/T snv 4.0E-06 0.800 1.000 2 1993 1994
dbSNP: rs1553609210
rs1553609210
THRB
4 0.851 0.040 3 24122984 missense variant C/T snv 0.700 1.000 2 1993 1994
dbSNP: rs121918693
rs121918693
THRB
2 0.925 0.040 3 24127684 missense variant C/A;T snv 0.700 0
dbSNP: rs121918697
rs121918697
THRB
4 0.882 0.040 3 24127631 missense variant G/A snv 0.700 0
dbSNP: rs121918709
rs121918709
THRB
1 1.000 0.040 3 24127634 missense variant T/C snv 0.700 0