List of variants in gene TNFRSF11A studied for Paget disease of bone 2, early-onset; Familial expansile osteolysis; Autosomal recessive osteopetrosis 7

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003839.4(TNFRSF11A):c.718A>G (p.Lys240Glu)	rs148185533	0.00066
NM_003839.4(TNFRSF11A):c.134G>A (p.Arg45Gln)	rs779581026	0.00001
NM_003839.4(TNFRSF11A):c.1054A>G (p.Arg352Gly)	rs2145355776
NM_003839.4(TNFRSF11A):c.637G>A (p.Gly213Ser)	rs766330561

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