"TNFSF11-related condition"[Disease/phenotype] AND "PreventionGenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 312227	NM_003701.4(TNFSF11):c.45G>A (p.Ser15=)	LOC130009662, TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 718598	NM_003701.4(TNFSF11):c.101C>G (p.Pro34Arg)	LOC130009662, TNFSF11 (P34R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 751927	NM_003701.4(TNFSF11):c.183C>A (p.Val61=)	TNFSF11	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 193255	NM_003701.4(TNFSF11):c.214G>A (p.Ala72Thr)	TNFSF11 (A72T)	Single nucleotide variant (missense variant +1 more)	TNFSF11-related condition +2 more	GConflicting classifications of pathogenicity
Select item 2634819	NM_003701.4(TNFSF11):c.387+1G>A	LOC126861752, TNFSF11	Single nucleotide variant (splice donor variant)	TNFSF11-related condition	GUncertain significance
Select item 1586069	NM_003701.4(TNFSF11):c.480T>C (p.Leu160=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	TNFSF11-related condition +1 more	GLikely benign
Select item 312235	NM_003701.4(TNFSF11):c.534T>C (p.Gly178=)	TNFSF11	Single nucleotide variant (synonymous variant)	TNFSF11-related condition +2 more	GConflicting classifications of pathogenicity

ClinVar