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
rs587777449
IFIH1
0.851 0.320 2 162282494 missense variant T/A;C snv 8.0E-06 6
rs748793969
DUOX2
0.827 0.120 15 45106327 missense variant G/A;T snv 3.2E-05; 6.8E-05 5
rs121908869
TSHR ; CEP128
0.882 0.160 14 80955802 missense variant G/C snv 4.0E-05 7.0E-06 5
rs121908866
TSHR ; LOC101928462
0.882 0.120 14 81143695 stop gained G/A snv 1.1E-04 2.0E-04 3
rs121908862
LOC101928462 ; TSHR
0.925 0.120 14 81092563 missense variant T/A snv 2
rs121908865
LOC101928462 ; TSHR
1.000 0.120 14 81087962 missense variant G/A snv 2.0E-05 7.0E-06 1
rs121908867
LOC101928462 ; TSHR
1.000 0.120 14 81143028 stop gained C/T snv 1
rs121908868
LOC101928462 ; TSHR
1.000 0.120 14 81143286 missense variant G/A snv 4.0E-06 1
rs121908870
LOC101928462 ; TSHR
1.000 0.120 14 81143633 missense variant C/A snv 1
rs121908871
LOC101928462 ; TSHR
1.000 0.120 14 81143228 missense variant T/G snv 1.6E-05 1.4E-05 1
rs121908881
LOC101928462 ; TSHR
1.000 0.120 14 81143488 missense variant C/T snv 4.0E-06 1
rs121908882
LOC101928462 ; TSHR
1.000 0.120 14 81142986 missense variant C/A;T snv 4.0E-06; 1.2E-05 1
rs121908884
LOC101928462 ; TSHR
1.000 0.120 14 81143856 missense variant T/C snv 1
rs121908885
LOC101928462 ; TSHR
1.000 0.120 14 81143458 missense variant T/C snv 1
rs142063461
LOC101928462 ; TSHR
1.000 0.120 14 81062179 missense variant C/T snv 5.4E-04 2.4E-04 1
rs786205080
LOC101928462 ; TSHR
1.000 0.120 14 81092611 splice region variant G/C snv 4.0E-06 7.0E-06 1
rs121908863
TSHR ; LOC101928462
1.000 0.120 14 81092547 missense variant C/A;G;T snv 4.0E-06; 1.4E-04 1
rs121908872
TSHR ; LOC101928462
1.000 0.120 14 81143715 missense variant G/A;T snv 3.2E-05; 8.0E-06 1