ClinVar Miner

List of variants reported as likely benign for spermatogenic failure 5 by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):

Infertility associated with multi-tailed spermatozoa and excessive DNA

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001015878.2(AURKC):c.396G>A (p.Leu132=)	rs55710619	0.00991
NM_001015878.2(AURKC):c.621G>A (p.Pro207=)	rs148940837	0.00593

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