List of variants in gene M1AP reported as pathogenic for spermatogenic failure

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001321739.2(M1AP):c.676dup (p.Trp226fs)	rs144217347	0.00238
NM_001321739.2(M1AP):c.797G>A (p.Arg266Gln)	rs149272394	0.00020
NM_001321739.2(M1AP):c.949G>A (p.Gly317Arg)	rs140179344	0.00006
NM_001321739.2(M1AP):c.1166C>T (p.Pro389Leu)	rs751126701	0.00001
NM_001321739.2(M1AP):c.1435-1G>A	rs1677697539

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