List of variants in gene DUSP6 reported as pathogenic for Kallmann syndrome

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_001946.4(DUSP6):c.566A>G (p.Asn189Ser)	rs143946794	0.00018
NM_001946.4(DUSP6):c.117C>A (p.Cys39Ter)	rs1879213059
NM_001946.4(DUSP6):c.229T>A (p.Phe77Ile)	rs587776978

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