List of variants in gene MOV10L1 reported as pathogenic for reproductive system disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_018995.3(MOV10L1):c.743+5G>A	rs367878826	0.00003
NM_018995.3(MOV10L1):c.2542G>A (p.Gly848Arg)	rs1278182234	0.00001
NM_018995.3(MOV10L1):c.2447G>T (p.Ser816Ile)	rs1479684172
NM_018995.3(MOV10L1):c.3095_3098del (p.Pro1032fs)	rs2147023849

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