FMNL1, formin like 1, 752

N. diseases: 27; N. variants: 2
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: rs12449792
rs12449792 		1.000 0.040 17 45224892 intron variant C/T snv 0.35
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2018 2018