List of variants in gene combination NANS, TRIM14 reported as uncertain significance for bone 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018946.4(NANS):c.709C>T (p.Arg237Cys)	rs878852982	0.00001
NM_018946.4(NANS):c.668T>C (p.Ile223Thr)	rs1587931148
NM_018946.4(NANS):c.937A>G (p.Thr313Ala)	rs140439077

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