List of variants in gene ORC6 reported as benign for Meier-Gorlin syndrome 3

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_014321.4(ORC6):c.675T>C (p.Asp225=)	rs34343511	0.01913
NM_014321.4(ORC6):c.*217C>T	rs143138864	0.00006
NM_014321.4(ORC6):c.*479G>A	rs533502054	0.00001
NM_014321.4(ORC6):c.360-13A>G	rs797045853

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