Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs189261858
LOC101928462 ; TSHR
0.776 0.160 14 81143407 missense variant G/A;T snv 2.3E-04 8
rs1555545033
THRA
0.807 0.160 17 40088306 missense variant C/T snv 7
rs748793969
DUOX2
0.827 0.120 15 45106327 missense variant G/A;T snv 3.2E-05; 6.8E-05 5
rs121918697
THRB
0.882 0.040 3 24127631 missense variant G/A snv 4
rs1553609210
THRB
0.851 0.040 3 24122984 missense variant C/T snv 4
rs121918690
THRB
0.882 0.040 3 24127694 missense variant C/T snv 3
rs121918695
THRB
0.882 0.080 3 24127696 missense variant C/T snv 4.0E-06 3
rs28933408
THRB
0.882 0.160 3 24122913 missense variant G/A;C;T snv 8.0E-06 3
rs758677446
LOC101927854 ; THRB
0.925 0.160 3 24190250 missense variant C/T snv 6.4E-05 7.0E-06 2
rs1405414838
RGR ; LRIT1
0.925 0.040 10 84232835 missense variant C/T snv 2
rs121918686
THRB
0.925 0.040 3 24127610 missense variant C/A;G;T snv 2
rs121918691
THRB
0.925 0.040 3 24122946 missense variant T/C snv 2
rs121918694
THRB
0.925 0.040 3 24143539 missense variant C/G;T snv 2
rs121918696
THRB
0.925 0.040 3 24127685 missense variant G/A snv 2
rs121918702
THRB
0.925 0.040 3 24122894 missense variant A/C snv 2
rs121918703
THRB
0.925 0.040 3 24122934 missense variant A/G snv 2
rs121918706
THRB
0.925 0.040 3 24143511 missense variant C/T snv 2
rs121918707
THRB
0.925 0.040 3 24143512 missense variant G/A;C snv 7.0E-06 2
rs121918708
THRB
0.925 0.040 3 24123122 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1267634673
THRB
0.925 0.040 3 24127628 missense variant C/T snv 2
rs1553609185
THRB
0.925 0.040 3 24122965 missense variant A/C snv 2
rs28999970
THRB
0.925 0.040 3 24127609 missense variant C/A;T snv 2
rs201391000
TXNRD2
0.925 0.080 22 19877157 missense variant C/A;T snv 2.3E-04 2
rs368176907
TXNRD2
1.000 0.040 22 19877158 missense variant G/A snv 2.8E-05 3.5E-05 2
rs142155451
LCOR
1.000 0.040 10 96982676 missense variant A/G snv 1.4E-05 1