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

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024715.4(TXNDC15):c.844C>T (p.Arg282Ter)	rs768237094	0.00001
NM_024715.4(TXNDC15):c.103+1G>A	rs886039792
NM_024715.4(TXNDC15):c.211dup (p.Gln71fs)	rs780024847
NM_024715.4(TXNDC15):c.635T>C (p.Leu212Pro)	rs760579409
NM_024715.4(TXNDC15):c.673_687del (p.Ser225_His229del)	rs886039791
NM_024715.4(TXNDC15):c.956dup (p.Ser321fs)	rs2150192064

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