List of variants in gene MKS1 reported as likely benign for central nervous system malformation

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017777.4(MKS1):c.1588+12C>G	rs762501967
NM_017777.4(MKS1):c.1600C>A (p.Arg534=)	rs772719574
NM_017777.4(MKS1):c.771G>A (p.Lys257=)	rs886038632

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