List of variants in gene TNFRSF11B reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002546.4(TNFRSF11B):c.401-5T>C	rs3134046	0.93049
NM_002546.4(TNFRSF11B):c.9C>G (p.Asn3Lys)	rs2073618	0.60108
NM_002546.4(TNFRSF11B):c.768A>G (p.Leu256=)	rs2228568	0.09806
NM_002546.4(TNFRSF11B):c.400+4C>T	rs1564858	0.09777
NM_002546.4(TNFRSF11B):c.817+8A>C	rs7844539	0.09748
NM_002546.4(TNFRSF11B):c.310G>A (p.Val104Met)	rs11573906	0.00021

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