List of variants in gene VAC14 reported as likely pathogenic for not provided

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_018052.5(VAC14):c.1895C>T (p.Thr632Met)	rs1060499667	0.00001
NM_018052.5(VAC14):c.2005G>T (p.Val669Leu)	rs1363536856	0.00001
NM_018052.5(VAC14):c.486+3A>G	rs1555527284
NM_018052.5(VAC14):c.595-10_595del	rs2033913406
NM_018052.5(VAC14):c.947-2A>G

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