Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704397
PDE8B
0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs189261858
LOC101928462 ; TSHR
0.776 0.160 14 81143407 missense variant G/A;T snv 2.3E-04 8
rs732609
TPO
0.827 0.160 2 1496155 missense variant A/C;G snv 0.43 5
rs121908869
TSHR ; CEP128
0.882 0.160 14 80955802 missense variant G/C snv 4.0E-05 7.0E-06 5
rs57659670
DUOX2
0.925 0.120 15 45106240 missense variant T/C snv 9.8E-02 0.17 2
rs753523115
SLC12A3
0.925 0.160 16 56880142 missense variant G/A snv 2.5E-05 7.0E-06 2
rs1294870139
TSHR ; LOC101928462
0.925 0.120 14 81143638 missense variant T/C snv 8.0E-06 2
rs139892516
TSHR ; LOC101928462
0.925 0.120 14 81143649 missense variant C/G;T snv 4.0E-06; 2.8E-05 2
rs200000982
DUOX2
1.000 0.040 15 45099449 missense variant T/C snv 6.0E-05 6.3E-05 1
rs61730030
DUOX2
1.000 0.040 15 45100816 missense variant G/A;C;T snv 4.0E-06; 5.0E-02; 1.2E-05 1