Disease: Hypothyroidism
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710
MAGEL2
0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs752746786
GNB1
0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs137854539
GNAS
0.716 0.520 20 58903703 missense variant C/T snv 27
rs1555570093
MPDU1
0.807 0.280 17 7586699 missense variant G/A snv 12