List of variants in gene MUTYH reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys)	rs150792276	0.00081
NM_001048174.2(MUTYH):c.914-9C>T	rs3219488	0.00045
NM_001048174.2(MUTYH):c.1464G>A (p.Pro488=)	rs143796254	0.00011
NM_001048174.2(MUTYH):c.612C>T (p.Thr204=)	rs780747266	0.00009
NM_001048174.2(MUTYH):c.1107G>T (p.Leu369=)	rs201412035	0.00007
NM_001048174.2(MUTYH):c.305-13C>G	rs201207780	0.00006
NM_001048174.2(MUTYH):c.900C>T (p.Asp300=)	rs587780752	0.00003
NM_001048174.2(MUTYH):c.116-75C>T	rs1481053395	0.00001
NM_001048174.2(MUTYH):c.705-20G>T	rs1645059942	0.00001
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=)	rs121908380

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