RAB5C, RAB5C, member RAS oncogene family, 5878

N. diseases: 24; N. variants: 18
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: rs12325861
rs12325861 		1.000 0.040 17 42137394 intron variant T/A;C snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019