Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs185398527
rs185398527
SLC30A2
CUI: C1842486
Disease: Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc
Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc 		0.720 GeneticVariation BEFREE Heterozygous mutations of human ZnT2 (hZnT2), including H54R and G87R, in mothers result in low (>75% reduction) secretion of zinc into the breast milk, and infants fed on the milk develop transient neonatal zinc deficiency. 23741301

2013
dbSNP: rs185398527
rs185398527
SLC30A2
CUI: C1842486
Disease: Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc
Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc 		0.720 GeneticVariation BEFREE A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency. 22733820

2012
dbSNP: rs185398527
rs185398527
SLC30A2
CUI: C1842486
Disease: Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc
Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc 		0.720 GeneticVariation UNIPROT