ClinVar Miner

List of variants reported as uncertain significance for central precocious puberty 1

Included ClinVar conditions (2):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_032551.5(KISS1R):c.890G>T (p.Arg297Leu)	rs144670595	0.00046
NM_032551.5(KISS1R):c.439C>T (p.Pro147Ser)	rs61735615	0.00001
NM_032551.5(KISS1R):c.244+6del

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