List of variants in gene TNFRSF11A reported as likely benign for autosomal recessive osteopetrosis

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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: 8

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HGVS	dbSNP	gnomAD frequency
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.*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.*633C>G	rs184568614
NM_003839.4(TNFRSF11A):c.*938T>C	rs565315471

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