List of variants in gene MGP reported as uncertain significance for bone disorder

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000900.4(MGP):c.-117C>T	rs569710471	0.00071
NM_000900.4(MGP):c.-66C>A	rs150994762	0.00043
NM_000900.5(MGP):c.234T>C (p.Leu78=)	rs149084241	0.00034
NM_000900.5(MGP):c.198C>T (p.His66=)	rs151158281	0.00024
NM_000900.5(MGP):c.84T>C (p.Ser28=)	rs886049107	0.00001
NM_000900.5(MGP):c.*176C>G	rs935518014
NM_000900.5(MGP):c.237C>T (p.Cys79=)	rs886049106
NM_000900.5(MGP):c.46G>A (p.Val16Ile)	rs868750856
NM_000900.5(MGP):c.62A>T (p.Glu21Val)
NM_000900.5(MGP):c.77T>C (p.Met26Thr)	rs754107566

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