List of variants in gene combination LOC126861465, MGP reported as uncertain significance 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.*476T>C	rs184916517	0.00017
NM_000900.5(MGP):c.*251T>C	rs886049105	0.00003
NM_000900.5(MGP):c.*531T>C	rs535008800	0.00001
NM_000900.5(MGP):c.*315dup	rs886049104
NM_000900.5(MGP):c.*455del	rs886049103
NM_000900.5(MGP):c.*720C>A	rs1032590657

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