PLXNC1, plexin C1, 10154

N. diseases: 29; N. variants: 12
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: rs3847803
rs3847803 		1.000 0.040 12 94164800 intron variant C/T snv 0.88
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019