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: rs1553609185
rs1553609185
THRB
2 0.925 0.040 3 24122965 missense variant A/C snv 0.700 0
dbSNP: rs28999970
rs28999970
THRB
2 0.925 0.040 3 24127609 missense variant C/A;T snv 0.700 0
dbSNP: rs121918695
rs121918695
THRB
3 0.882 0.080 3 24127696 missense variant C/T snv 4.0E-06 0.010 < 0.001 1 1994 1994
dbSNP: rs201391000
rs201391000
TXNRD2
2 0.925 0.080 22 19877157 missense variant C/A;T snv 2.3E-04 0.010 < 0.001 1 1994 1994
dbSNP: rs748793969
rs748793969
DUOX2
5 0.827 0.120 15 45106327 missense variant G/A;T snv 3.2E-05; 6.8E-05 0.010 1.000 1 2017 2017
dbSNP: rs28933408
rs28933408
THRB
3 0.882 0.160 3 24122913 missense variant G/A;C;T snv 8.0E-06 0.060 1.000 6 1994 2019
dbSNP: rs1555545033
rs1555545033
THRA
7 0.807 0.160 17 40088306 missense variant C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs189261858
rs189261858
TSHR ; LOC101928462
8 0.776 0.160 14 81143407 missense variant G/A;T snv 2.3E-04 0.010 1.000 1 2006 2006
dbSNP: rs758677446
rs758677446
THRB ; LOC101927854
2 0.925 0.160 3 24190250 missense variant C/T snv 6.4E-05 7.0E-06 0.010 1.000 1 2019 2019