C1835171[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 755271	NM_001680.5(FXYD2):c.198G>A (p.Pro66=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	Renal hypomagnesemia 2 +1 more	GLikely benign
Select item 724848	NM_001680.5(FXYD2):c.198G>T (p.Pro66=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	Renal hypomagnesemia 2 +1 more	GBenign/Likely benign
Select item 302522	NM_001680.5(FXYD2):c.195G>A (p.Glu65=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	Renal hypomagnesemia 2 +1 more	GBenign
Select item 302523	NM_001680.5(FXYD2):c.183C>T (p.Ile61=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	Renal hypomagnesemia 2 +1 more	GBenign/Likely benign
Select item 1489687	NM_001680.5(FXYD2):c.176G>A (p.Arg59Lys)	FXYD2, FXYD6-FXYD2 (R59K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 719221	NM_001680.5(FXYD2):c.126C>T (p.Leu42=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 789041	NM_001680.5(FXYD2):c.114C>T (p.Phe38=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 736288	NM_001680.5(FXYD2):c.110C>A (p.Ala37Asp)	FXYD2, FXYD6-FXYD2 (A37D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +3 more	GLikely benign
Select item 879279	NM_001680.5(FXYD2):c.90C>T (p.Gly30=)	FXYD2, FXYD6-FXYD2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 302526	NM_001680.5(FXYD2):c.28G>A (p.Gly10Ser)	FXYD2, FXYD6-FXYD2 (G10S +3 more)	Single nucleotide variant (missense variant)	FXYD2-related disorder +2 more	GConflicting classifications of pathogenicity