List of variants in gene TMPRSS3 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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_001256317.3(TMPRSS3):c.412G>A (p.Ala138Thr)	rs140614903	0.00054
NM_001256317.3(TMPRSS3):c.1126G>A (p.Gly376Ser)	rs371448615	0.00011
NM_001256317.3(TMPRSS3):c.1177G>A (p.Val393Met)	rs151315833	0.00002
NM_001256317.3(TMPRSS3):c.496C>T (p.Arg166Trp)	rs781395690	0.00001

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