Variants in gene TMPRSS3 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.239G>A (p.Arg80His)	rs146159479	0.00013
NM_001256317.3(TMPRSS3):c.326G>A (p.Arg109Gln)	rs139484231	0.00009
NM_001256317.3(TMPRSS3):c.595G>A (p.Val199Met)	rs772040483	0.00004
NM_001256317.3(TMPRSS3):c.1148T>A (p.Met383Lys)	rs749798053	0.00002
NM_001256317.3(TMPRSS3):c.1149G>T (p.Met383Ile)	rs727503492
NM_001256317.3(TMPRSS3):c.1180G>C (p.Asp394His)	rs111033537
NM_001256317.3(TMPRSS3):c.1333G>A (p.Glu445Lys)

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