List of variants in gene MYPN studied for Primary familial hypertrophic cardiomyopathy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.3124C>T (p.Arg1042Cys)	rs151282801	0.00034
NM_032578.4(MYPN):c.2642A>T (p.Asn881Ile)	rs71584493	0.00007
NM_032578.4(MYPN):c.2114C>T (p.Thr705Ile)	rs768471574	0.00001
NM_032578.4(MYPN):c.35T>C (p.Ile12Thr)	rs869025490	0.00001
NM_032578.4(MYPN):c.3697A>T (p.Ile1233Phe)	rs587782969	0.00001
NM_032578.4(MYPN):c.101G>A (p.Arg34Gln)	rs730880168
NM_032578.4(MYPN):c.2981T>G (p.Met994Arg)	rs786205348
NM_032578.4(MYPN):c.970C>T (p.His324Tyr)	rs1589550119

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