List of variants reported as likely pathogenic for Meckel syndrome by Natera, Inc.

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_017777.4(MKS1):c.190+2T>C	rs375170572	0.00004
NM_017777.4(MKS1):c.417+1G>A	rs756368560

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