List of variants in gene CFAP69 reported as pathogenic for Spermatogenic failure 24

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001039706.3(CFAP69):c.647G>A (p.Trp216Ter)	rs1355278372	0.00001
NM_001039706.3(CFAP69):c.1069_1070insAC (p.Leu357fs)	rs764048407
NM_001039706.3(CFAP69):c.763C>T (p.Gln255Ter)	rs1554359569
NM_001039706.3(CFAP69):c.860+1G>A	rs1554359685

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