List of variants in gene MGP reported as benign for Keutel syndrome

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000900.5(MGP):c.304A>G (p.Thr102Ala)	rs4236	0.41895
NM_000900.5(MGP):c.-63G>A	rs1800801	0.32542
NM_000900.5(MGP):c.157A>G (p.Lys53Glu)	rs1801716	0.00329
NM_000900.5(MGP):c.23C>T (p.Ala8Val)	rs142330429	0.00171
NM_000900.5(MGP):c.*27T>G	rs80337043	0.00164
NM_000900.5(MGP):c.62-18dup	rs11393307

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