C0029456[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 974971	NM_000478.6(ALPL):c.94C>T (p.Gln32Ter)	ALPL (Q32*)	Single nucleotide variant (nonsense +1 more)	Osteoporosis +3 more	GPathogenic/Likely pathogenic
Select item 1708283	NM_005430.4(WNT1):c.465C>A (p.Tyr155Ter)	WNT1 (Y155*)	Single nucleotide variant (nonsense)	Osteoporosis	GPathogenic
Select item 1691560	NM_000138.5(FBN1):c.6170G>A (p.Arg2057Gln)	FBN1 (R2057Q)	Single nucleotide variant (missense variant)	Osteoporosis	GUncertain significance

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