ClinVar Miner

List of variants in gene TGM1 reported as likely pathogenic by Genetics and Molecular Pathology, SA Pathology

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000359.3(TGM1):c.420A>G (p.Ile140Met)	rs139208806	0.00008
NM_000359.3(TGM1):c.814T>C (p.Ser272Pro)	rs764040146

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