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

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_016628.5(WAC):c.1198C>T (p.Gln400Ter)	rs1064796758
NM_016628.5(WAC):c.1437+1G>A	rs1554791124
NM_016628.5(WAC):c.1556+2T>G	rs1841399401
NM_016628.5(WAC):c.1589del (p.His530fs)	rs2492209822
NM_016628.5(WAC):c.1722G>A (p.Trp574Ter)	rs1841465878
NM_016628.5(WAC):c.1820del (p.Asn607fs)	rs886041564
NM_016628.5(WAC):c.1870C>T (p.Gln624Ter)

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