List of variants in gene MYPN reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.1245+20A>G	rs111634581	0.00919
NM_032578.4(MYPN):c.1079-18T>C	rs114932559	0.00278
NM_032578.4(MYPN):c.1460-14T>A	rs201156035	0.00096
NM_032578.4(MYPN):c.1236C>A (p.Thr412=)	rs151220474	0.00058
NM_032578.4(MYPN):c.2190G>A (p.Thr730=)	rs71584492	0.00040
NM_032578.4(MYPN):c.2742T>C (p.Asn914=)	rs372375235	0.00011
NM_032578.4(MYPN):c.2925+20A>C	rs200111945	0.00005
NM_032578.4(MYPN):c.3456C>T (p.Thr1152=)	rs202183926	0.00005
NM_032578.4(MYPN):c.2565-7C>T	rs373241021	0.00004
NM_032578.4(MYPN):c.3006C>T (p.Cys1002=)	rs1321971649	0.00003
NM_032578.4(MYPN):c.3441C>T (p.Ile1147=)	rs759420426	0.00003
NM_032578.4(MYPN):c.2704-13G>A	rs1381527530	0.00001
NM_032578.4(MYPN):c.3159-19A>C	rs754950593	0.00001

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