List of variants in gene ORC1 reported as likely benign for Meier-Gorlin syndrome 1

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004153.4(ORC1):c.806C>T (p.Ser269Leu)	rs61753390	0.00642
NM_004153.4(ORC1):c.2314G>A (p.Val772Ile)	rs61753389	0.00503
NM_004153.4(ORC1):c.57G>C (p.Arg19Ser)	rs3087473	0.00436
NM_004153.4(ORC1):c.2226C>A (p.Ser742=)	rs34644009	0.00269
NM_004153.4(ORC1):c.402+12C>T	rs138085865	0.00193
NM_004153.4(ORC1):c.403-7A>C	rs199834691	0.00190
NM_004153.4(ORC1):c.1745A>G (p.Gln582Arg)	rs547441862	0.00061
NM_004153.4(ORC1):c.608C>T (p.Thr203Ile)	rs202095223	0.00005
NM_004153.4(ORC1):c.189G>T (p.Pro63=)	rs201244952

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