List of variants in gene TNFRSF11A reported as benign for Paget disease of bone 2, early-onset

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_003839.4(TNFRSF11A):c.*2590A>C	rs884205	0.81374
NM_003839.4(TNFRSF11A):c.*1624G>C	rs12455323	0.18364
NM_003839.4(TNFRSF11A):c.*2490A>G	rs78459945	0.12123
NM_003839.4(TNFRSF11A):c.*2173A>T	rs78326403	0.11998
NM_003839.4(TNFRSF11A):c.*2537G>A	rs72933641	0.07811
NM_003839.4(TNFRSF11A):c.*1810G>C	rs72933640	0.07294
NM_003839.4(TNFRSF11A):c.*1913A>G	rs12721435	0.01660
NM_003839.4(TNFRSF11A):c.625G>A (p.Val209Ile)	rs146793660	0.00253
NM_003839.4(TNFRSF11A):c.*1269G>C	rs115023470
NM_003839.4(TNFRSF11A):c.*634C>G	rs7232657

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