List of variants in gene MOV10L1 reported as uncertain significance for male infertility

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018995.3(MOV10L1):c.2258T>C (p.Val753Ala)
NM_018995.3(MOV10L1):c.3115G>A (p.Glu1039Lys)
NM_018995.3(MOV10L1):c.3268G>T (p.Val1090Phe)

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