List of variants in gene SLC11A1 reported as likely benign for SLC11A1-related disorder

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000578.4(SLC11A1):c.875T>C (p.Leu292Pro)	rs145536242	0.00125
NM_000578.4(SLC11A1):c.1143C>T (p.Tyr381=)	rs191066713	0.00033
NM_000578.4(SLC11A1):c.870C>T (p.Ile290=)	rs560129385	0.00005
NM_000578.4(SLC11A1):c.796-4G>A	rs767192438	0.00003
NM_000578.4(SLC11A1):c.796-5C>T	rs374719609	0.00002

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