List of variants in gene TNFRSF11A reported as likely benign for bone disorder

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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: 20

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HGVS	dbSNP	gnomAD frequency
NM_003839.4(TNFRSF11A):c.933A>G (p.Thr311=)	rs8092336	0.95903
NM_003839.4(TNFRSF11A):c.575C>T (p.Ala192Val)	rs1805034	0.56701
NM_003839.4(TNFRSF11A):c.421C>T (p.His141Tyr)	rs35211496	0.12362
NM_003839.4(TNFRSF11A):c.75+5G>A	rs146553439	0.02406
NM_003839.4(TNFRSF11A):c.*668G>T	rs78622775	0.01625
NM_003839.4(TNFRSF11A):c.1397G>A (p.Arg466His)	rs35993683	0.01070
NM_003839.4(TNFRSF11A):c.*1738C>T	rs6567277	0.00718
NM_003839.4(TNFRSF11A):c.1519G>A (p.Ala507Thr)	rs61751992	0.00618
NM_003839.4(TNFRSF11A):c.570C>T (p.Ser190=)	rs12721430	0.00322
NM_003839.4(TNFRSF11A):c.*2077G>T	rs75853662	0.00278
NM_003839.4(TNFRSF11A):c.1348C>T (p.Arg450Trp)	rs34945627	0.00239
NM_003839.4(TNFRSF11A):c.284-5C>T	rs371545302	0.00130
NM_003839.4(TNFRSF11A):c.*1060C>T	rs572639953	0.00100
NM_003839.4(TNFRSF11A):c.1567+7G>A	rs35332936	0.00011
NM_003839.4(TNFRSF11A):c.*2086G>A	rs528958493	0.00001
NM_003839.4(TNFRSF11A):c.*1251dup	rs150401931
NM_003839.4(TNFRSF11A):c.*320del	rs552069161
NM_003839.4(TNFRSF11A):c.*633C>G	rs184568614
NM_003839.4(TNFRSF11A):c.634_635dup	rs142942284
NM_003839.4(TNFRSF11A):c.*938T>C	rs565315471

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