ClinVar Miner

List of variants in gene combination LRRC41, RAD54L reported as likely pathogenic for premature ovarian failure 1

Included ClinVar conditions (4):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003579.4(RAD54L):c.1900C>T (p.Arg634Cys)	rs368491231	0.00002
NM_003579.4(RAD54L):c.1883A>C (p.Glu628Ala)	rs1660658865

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