"Genome Diagnostics Laboratory, The Hospital for Sick Children"[submit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 193256	NM_003701.4(TNFSF11):c.80A>G (p.Glu27Gly)	LOC130009662, TNFSF11 (E27G)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GBenign
Select item 312229	NM_003701.4(TNFSF11):c.107C>G (p.Pro36Arg)	LOC130009662, TNFSF11 (P36R)	Single nucleotide variant (missense variant +1 more)	Increased bone mineral density +3 more	GBenign/Likely benign
Select item 312231	NM_003701.4(TNFSF11):c.239C>T (p.Ser80Leu)	LOC126861752, TNFSF11 (S7L +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 716176	NM_003701.4(TNFSF11):c.396A>G (p.Gln132=)	LOC126861753, TNFSF11	Single nucleotide variant (synonymous variant)	Autosomal recessive osteopetrosis 2 +2 more	GBenign
Select item 1701974	NM_003701.4(TNFSF11):c.704A>G (p.Tyr235Cys)	TNFSF11 (Y162C +1 more)	Single nucleotide variant (missense variant)	Increased bone mineral density	GUncertain significance
Select item 312237	NM_003701.4(TNFSF11):c.924T>C (p.Phe308=)	TNFSF11	Single nucleotide variant (synonymous variant)	Increased bone mineral density +2 more	GBenign

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