Gene: TSHR ×
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: rs121908873
rs121908873
TSHR ; LOC101928462
7 0.790 0.160 14 81139828 missense variant G/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs121908874
rs121908874
TSHR ; LOC101928462
7 0.807 0.080 14 81143584 missense variant T/C snv 0.010 1.000 1 1994 1994
dbSNP: rs121908875
rs121908875
TSHR ; LOC101928462
2 0.925 0.040 14 81144073 missense variant G/A snv 0.010 1.000 1 1994 1994
dbSNP: rs121908879
rs121908879
TSHR ; LOC101928462
2 0.925 0.080 14 81096641 missense variant A/G snv 0.010 1.000 1 2002 2002
dbSNP: rs1991517
rs1991517
TSHR ; LOC101928462
13 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 < 0.001 1 2016 2016
dbSNP: rs28937584
rs28937584
TSHR ; LOC101928462
4 0.925 0.080 14 81143955 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs571893270
rs571893270
TSHR ; LOC101928462
3 0.882 0.040 14 81143641 missense variant G/A snv 8.0E-05 2.1E-05 0.010 1.000 1 1998 1998