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: 12

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HGVS	dbSNP	gnomAD frequency
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.1340T>C (p.Met447Thr)	rs201018751	0.00001
NM_001256317.3(TMPRSS3):c.1028G>T (p.Trp343Leu)
NM_001256317.3(TMPRSS3):c.1149G>T (p.Met383Ile)	rs727503492
NM_001256317.3(TMPRSS3):c.1157C>T (p.Ala386Val)
NM_001256317.3(TMPRSS3):c.1303C>T (p.Arg435Cys)	rs565348874
NM_001256317.3(TMPRSS3):c.1304G>A (p.Arg435His)
NM_001256317.3(TMPRSS3):c.1333G>A (p.Glu445Lys)
NM_001256317.3(TMPRSS3):c.238C>T (p.Arg80Cys)	rs143733205
NM_001256317.3(TMPRSS3):c.274T>C (p.Cys92Arg)

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