Disease: Hypothyroidism
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 2