C1QTNF6, C1q and TNF related 6, 114904

N. diseases: 33; N. variants: 5
Disease: Hypothyroidism ×
Source: ALL
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: rs229540
rs229540 		1.000 0.040 22 37195250 intron variant T/G snv 0.49
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019