ammonium acutifolium - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 5750	NM_003059.3(SLC22A4):c.1507C>T (p.Leu503Phe)	MIR3936HG, SLC22A4 (L503F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2244914	NM_000324.3(RHAG):c.1108G>A (p.Gly370Arg)	RHAG (G370R)	Single nucleotide variant (missense variant)	Rh-null, regulator type +1 more	GConflicting classifications of pathogenicity
Select item 2573392	NM_000324.3(RHAG):c.827C>G (p.Thr276Ser)	RHAG (T276S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2577270	NM_000324.3(RHAG):c.572G>A (p.Arg191Gln)	RHAG (R191Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 218295	NM_000324.3(RHAG):c.194T>C (p.Phe65Ser)	RHAG (F65S)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 16125	NM_005271.5(GLUD1):c.1496G>A (p.Gly499Asp)	GLUD1 (G499D +2 more)	Single nucleotide variant (missense variant)	Hyperinsulinism-hyperammonemia syndrome	GPathogenic
Select item 16124	NM_005271.5(GLUD1):c.1495G>A (p.Gly499Ser)	GLUD1 (G499S +2 more)	Single nucleotide variant (missense variant)	Hyperinsulinism-hyperammonemia syndrome	GUncertain significance
Select item 222028	NM_000334.4(SCN4A):c.4609G>A (p.Gly1537Ser)	GH-LCR, SCN4A (G1537S)	Single nucleotide variant (missense variant)	Familial hyperkalemic periodic paralysis +6 more	GUncertain significance

ClinVar