PVT1, Pvt1 oncogene, 5820

N. diseases: 27; N. variants: 31
Disease: Hypothyroidism ×
Source: GWASCAT ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10956412
rs10956412 		1.000 0.040 8 128150251 intron variant A/C;G snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019