"SLC11A1-related condition"[Disease/phenotype] AND "PreventionGenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055747	NM_000578.4(SLC11A1):c.115C>T (p.Leu39=)	SLC11A1	Single nucleotide variant (synonymous variant)	SLC11A1-related condition	GBenign
Select item 3055354	NM_000578.4(SLC11A1):c.747C>T (p.Gly249=)	SLC11A1	Single nucleotide variant (synonymous variant)	SLC11A1-related condition	GBenign
Select item 3040629	NM_000578.4(SLC11A1):c.796-5C>T	SLC11A1	Single nucleotide variant (intron variant)	SLC11A1-related condition	GLikely benign
Select item 3035428	NM_000578.4(SLC11A1):c.796-4G>A	SLC11A1	Single nucleotide variant (intron variant)	SLC11A1-related condition	GLikely benign
Select item 3040630	NM_000578.4(SLC11A1):c.870C>T (p.Ile290=)	SLC11A1	Single nucleotide variant (synonymous variant)	SLC11A1-related condition	GLikely benign
Select item 3033569	NM_000578.4(SLC11A1):c.875T>C (p.Leu292Pro)	SLC11A1 (L292P)	Single nucleotide variant (missense variant)	SLC11A1-related condition	GLikely benign
Select item 3045914	NM_000578.4(SLC11A1):c.1143C>T (p.Tyr381=)	SLC11A1	Single nucleotide variant (synonymous variant)	SLC11A1-related condition	GLikely benign
Select item 3035789	NM_000578.4(SLC11A1):c.1256G>A (p.Arg419Gln)	SLC11A1 (R419Q)	Single nucleotide variant (missense variant)	SLC11A1-related condition	GBenign
Select item 731804	NM_000578.4(SLC11A1):c.1492G>A (p.Gly498Ser)	SLC11A1 (G498S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign

ClinVar