"PreventionGenetics, part of Exact Sciences"[submitter] AND "SOST"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051959	NM_025237.3(SOST):c.448G>C (p.Gly150Arg)	SOST (G150R)	Single nucleotide variant (missense variant)	SOST-related disorder	GLikely benign
Select item 2637182	NM_025237.3(SOST):c.350A>G (p.Asn117Ser)	SOST (N117S)	Single nucleotide variant (missense variant)	SOST-related disorder	GUncertain significance
Select item 747371	NM_025237.3(SOST):c.198C>T (p.Pro66=)	SOST	Single nucleotide variant (synonymous variant)	SOST-related disorder +1 more	GLikely benign
Select item 31592	NM_025237.3(SOST):c.61G>A (p.Val21Met)	SOST (V21M)	Single nucleotide variant (missense variant)	SOST-related disorder	GLikely pathogenic
Select item 890596	NM_025237.3(SOST):c.56G>A (p.Arg19His)	SOST (R19H)	Single nucleotide variant (missense variant)	Sclerosteosis 1 +2 more	GLikely benign
Select item 193461	NM_025237.3(SOST):c.-10G>A	SOST	Single nucleotide variant (5 prime UTR variant)	Sclerosteosis 1 +2 more	GBenign/Likely benign

ClinVar