List of variants in gene MYH7 reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu)	rs45496496	0.00050
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro)	rs372731424	0.00010
NM_000257.4(MYH7):c.1322C>T (p.Thr441Met)	rs121913653	0.00006
NM_000257.4(MYH7):c.632C>T (p.Pro211Leu)	rs727503277	0.00002
NM_000257.4(MYH7):c.1447G>A (p.Glu483Lys)	rs121913651	0.00001
NM_000257.4(MYH7):c.3152C>T (p.Ala1051Val)	rs727504358	0.00001
NM_000257.4(MYH7):c.1748C>T (p.Ala583Val)	rs2138672244
NM_000257.4(MYH7):c.323G>A (p.Arg108His)	rs730880832
NM_000257.4(MYH7):c.3337-4dup	rs45504498
NM_000257.4(MYH7):c.3621C>G (p.Ile1207Met)	rs529700838
NM_000257.4(MYH7):c.3748C>G (p.Arg1250Gly)	rs727503249
NM_000257.4(MYH7):c.715G>A (p.Asp239Asn)	rs397516264
NM_000257.4(MYH7):c.746G>T (p.Arg249Leu)	rs3218713

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