SLC39A8, solute carrier family 39 member 8, 64116

N. diseases: 138; N. variants: 19
Disease: Heart failure ×
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: rs13114738
rs13114738 		0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.700 1.000 1 2016 2016