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: rs12101255
rs12101255
TSHR
2 0.925 0.120 14 80984708 intron variant C/T snv 0.37 0.010 1.000 1 2012 2012
dbSNP: rs179247
rs179247
TSHR
5 0.882 0.160 14 80966202 intron variant A/G snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs1991517
rs1991517
TSHR ; LOC101928462
13 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 0.010 1.000 1 2014 2014
dbSNP: rs2268458
rs2268458
TSHR
2 0.925 0.120 14 80996551 intron variant T/C snv 0.20 0.010 1.000 1 2008 2008
dbSNP: rs3783938
rs3783938
TSHR ; LOC101928462
2 0.925 0.120 14 81128036 intron variant C/T snv 0.13 0.010 1.000 1 2012 2012
dbSNP: rs4411444
rs4411444
TSHR
2 0.925 0.120 14 80978764 intron variant A/G snv 0.43 0.010 1.000 1 2017 2017
dbSNP: rs4903961
rs4903961
TSHR
2 0.925 0.120 14 80996305 intron variant C/G snv 0.39 0.010 1.000 1 2017 2017