MB21D2, Mab-21 domain containing 2, 151963

N. diseases: 6; N. variants: 3
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: rs12485900
rs12485900 		1.000 0.040 3 192905990 intron variant C/A;T snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019