List of variants in gene TNFRSF11A reported as uncertain significance for Familial expansile osteolysis

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_003839.4(TNFRSF11A):c.1703G>A (p.Arg568His)	rs375618864	0.00034
NM_003839.4(TNFRSF11A):c.1370G>A (p.Cys457Tyr)	rs1910343501
NM_003839.4(TNFRSF11A):c.1442AAG[2] (p.Glu483del)
NM_003839.4(TNFRSF11A):c.1544C>A (p.Pro515His)	rs2145358021
NM_003839.4(TNFRSF11A):c.338C>T (p.Ala113Val)	rs1909092200

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