List of variants in gene MYPN reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg)	rs62620248	0.01839
NM_032578.4(MYPN):c.2925+9G>C	rs12241644	0.01362
NM_032578.4(MYPN):c.3279C>T (p.Asp1093=)	rs115033934	0.01152
NM_032578.4(MYPN):c.2447C>T (p.Pro816Leu)	rs111965755	0.01059
NM_032578.4(MYPN):c.1245+20A>G	rs111634581	0.00919
NM_032578.4(MYPN):c.3493+11C>T	rs113674647	0.00520
NM_032578.4(MYPN):c.1134C>T (p.Ile378=)	rs145701607	0.00504
NM_032578.4(MYPN):c.3078G>A (p.Gly1026=)	rs114479328	0.00385
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile)	rs138313730	0.00123

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