List of variants in gene MARVELD2 reported as likely pathogenic for not provided

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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_001038603.3(MARVELD2):c.1147-2A>G	rs763062791	0.00001
NM_001038603.3(MARVELD2):c.296G>A (p.Trp99Ter)	rs993107184	0.00001
NM_001038603.3(MARVELD2):c.490C>T (p.Arg164Ter)	rs748896801	0.00001
NM_001038603.3(MARVELD2):c.1203del (p.Asp402fs)
NM_001038603.3(MARVELD2):c.595del (p.Val199fs)	rs1554046316
NM_001038603.3(MARVELD2):c.880_890del (p.Phe294fs)	rs770042200

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