List of variants in gene combination LOC126860797, NSMF reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001130969.3(NSMF):c.1435A>G (p.Arg479Gly)	rs1174502792	0.00001
NM_001130969.3(NSMF):c.1261C>T (p.Leu421Phe)	rs1588492186

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