List of variants in gene CFAP410 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004928.3(CFAP410):c.347C>T (p.Pro116Leu)	rs922930539	0.00003
NM_004928.3(CFAP410):c.286G>A (p.Glu96Lys)	rs774614339	0.00002
NM_004928.3(CFAP410):c.218G>C (p.Arg73Pro)	rs140451304
NM_004928.3(CFAP410):c.443_444del (p.Glu148fs)	rs756970705
NM_004928.3(CFAP410):c.78-2del	rs749801652
NM_004928.3(CFAP410):c.96+4del	rs1268187387
NM_004928.3(CFAP410):c.97-1G>A

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