List of variants in gene combination COMT, TXNRD2 reported as likely benign for Primary dilated cardiomyopathy

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_006440.5(TXNRD2):c.21G>A (p.Ala7=)	rs2146120385
NM_006440.5(TXNRD2):c.21G>C (p.Ala7=)
NM_006440.5(TXNRD2):c.6G>C (p.Ala2=)	rs1601501125
NM_006440.5(TXNRD2):c.6G>T (p.Ala2=)	rs1601501125

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