List of variants in gene TXNDC15 reported as likely pathogenic for Meckel syndrome

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_024715.4(TXNDC15):c.103+1G>A	rs886039792
NM_024715.4(TXNDC15):c.673_687del (p.Ser225_His229del)	rs886039791

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