List of variants in gene KLHL10 reported as uncertain significance for Spermatogenic failure 11

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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_152467.5(KLHL10):c.647A>C (p.Gln216Pro)	rs116420871	0.00348
NM_152467.5(KLHL10):c.937G>A (p.Ala313Thr)	rs370756367	0.00042
NM_152467.5(KLHL10):c.923T>C (p.Ile308Thr)	rs377399919	0.00005
NM_152467.5(KLHL10):c.1014A>C (p.Lys338Asn)	rs2544489279

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