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: rs121918686
rs121918686
THRB
2 0.925 0.040 3 24127610 missense variant C/A;G;T snv 0.800 1.000 19 1989 2009
dbSNP: rs121918687
rs121918687
THRB
1 1.000 0.040 3 24122912 missense variant G/T snv 0.800 1.000 19 1989 2009
dbSNP: rs121918688
rs121918688
THRB
1 1.000 0.040 3 24127623 missense variant C/G;T snv 4.0E-06 0.800 1.000 19 1989 2009
dbSNP: rs121918690
rs121918690
THRB
3 0.882 0.040 3 24127694 missense variant C/T snv 0.800 1.000 19 1989 2009
dbSNP: rs121918691
rs121918691
THRB
2 0.925 0.040 3 24122946 missense variant T/C snv 0.800 1.000 19 1989 2009
dbSNP: rs121918692
rs121918692
THRB
1 1.000 0.040 3 24122943 missense variant T/C snv 0.800 1.000 19 1989 2009
dbSNP: rs121918693
rs121918693
THRB
2 0.925 0.040 3 24127684 missense variant C/A;T snv 0.800 1.000 19 1989 2009
dbSNP: rs121918694
rs121918694
THRB
2 0.925 0.040 3 24143539 missense variant C/G;T snv 0.800 1.000 19 1989 2009
dbSNP: rs121918696
rs121918696
THRB
2 0.925 0.040 3 24127685 missense variant G/A snv 0.800 1.000 19 1989 2009
dbSNP: rs121918697
rs121918697
THRB
4 0.882 0.040 3 24127631 missense variant G/A snv 0.800 1.000 19 1989 2009
dbSNP: rs121918698
rs121918698
THRB
1 1.000 0.040 3 24122957 missense variant C/T snv 7.0E-06 0.800 1.000 19 1989 2009
dbSNP: rs121918703
rs121918703
THRB
2 0.925 0.040 3 24122934 missense variant A/G snv 0.800 1.000 19 1989 2009
dbSNP: rs121918707
rs121918707
THRB
2 0.925 0.040 3 24143512 missense variant G/A;C snv 7.0E-06 0.800 1.000 19 1989 2009
dbSNP: rs28933408
rs28933408
THRB
3 0.882 0.160 3 24122913 missense variant G/A;C;T snv 8.0E-06 0.800 1.000 19 1989 2009
dbSNP: rs28999969
rs28999969
THRB
1 1.000 0.040 3 24127649 missense variant C/T snv 0.800 1.000 19 1989 2009
dbSNP: rs28999970
rs28999970
THRB
2 0.925 0.040 3 24127609 missense variant C/A;T snv 0.800 1.000 19 1989 2009
dbSNP: rs28999971
rs28999971
THRB
1 1.000 0.040 3 24127603 missense variant C/T snv 0.800 1.000 19 1989 2009
dbSNP: rs121918702
rs121918702
THRB
2 0.925 0.040 3 24122894 missense variant A/C snv 0.700 1.000 19 1989 2009
dbSNP: rs1553609195
rs1553609195
THRB
1 1.000 0.040 3 24122977 missense variant T/C snv 0.700 1.000 19 1989 2009
dbSNP: rs1057519028
rs1057519028
THRB
1 1.000 0.040 3 24122919 missense variant A/C;G snv 0.700 0
dbSNP: rs1060499695
rs1060499695
THRB
1 1.000 0.040 3 24127666 missense variant T/C snv 0.700 0
dbSNP: rs121918704
rs121918704
THRB
2 0.925 0.040 3 24122897 missense variant A/G snv 0.700 0
dbSNP: rs121918705
rs121918705
THRB
1 1.000 0.040 3 24122968 stop gained G/T snv 0.700 0
dbSNP: rs121918706
rs121918706
THRB
2 0.925 0.040 3 24143511 missense variant C/T snv 0.700 0
dbSNP: rs121918708
rs121918708
THRB
2 0.925 0.040 3 24123122 missense variant C/T snv 4.0E-06 7.0E-06 0.700 0