List of variants in gene combination LOC130066960, TXNRD2 reported as benign for Primary dilated cardiomyopathy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006440.5(TXNRD2):c.103+19G>A	rs45536341	0.00329
NM_006440.5(TXNRD2):c.103+14dup	rs756452923
NM_006440.5(TXNRD2):c.68C>A (p.Ala23Glu)	rs532340383

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