Variants in gene TMPRSS3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.-34G>A	rs73372256	0.05210
NM_001256317.3(TMPRSS3):c.268G>A (p.Ala90Thr)	rs45598239	0.03352
NM_001256317.3(TMPRSS3):c.432A>G (p.Gln144=)	rs61731564	0.02161
NM_001256317.3(TMPRSS3):c.*246G>A	rs57692239	0.00691
NM_001256317.3(TMPRSS3):c.1119C>T (p.Asp373=)	rs113747896	0.00291
NM_001256317.3(TMPRSS3):c.1125C>T (p.Tyr375=)	rs111033292	0.00235
NM_001256317.3(TMPRSS3):c.957G>C (p.Met319Ile)	rs115223836	0.00229
NM_001256317.3(TMPRSS3):c.933C>T (p.Ala311=)	rs145235893	0.00153
NM_001256317.3(TMPRSS3):c.231C>T (p.Tyr77=)	rs139934512	0.00125
NM_001256317.3(TMPRSS3):c.715T>C (p.Tyr239His)	rs149001183	0.00109
NM_001256317.3(TMPRSS3):c.1332C>T (p.His444=)	rs186972955	0.00066
NM_001256317.3(TMPRSS3):c.681G>A (p.Gln227=)	rs201260442	0.00013
NM_001256317.3(TMPRSS3):c.1191+10C>T	rs201451028	0.00012
NM_001256317.3(TMPRSS3):c.323-8T>C	rs201482591	0.00006

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