List of variants in gene TMPRSS6 reported as likely pathogenic for not provided

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001374504.1(TMPRSS6):c.1038C>A (p.Tyr346Ter)	rs137853121	0.00001
NM_001374504.1(TMPRSS6):c.1768C>T (p.Arg590Ter)	rs137853123	0.00001
NM_001374504.1(TMPRSS6):c.1442-2A>G
NM_001374504.1(TMPRSS6):c.2407T>G (p.Ter803Gly)	rs2146016503

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