List of variants in gene MYH7 reported as likely pathogenic for Dilated cardiomyopathy 1S

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1325G>A (p.Arg442His)	rs730880870	0.00003
NM_000257.4(MYH7):c.1491G>T (p.Glu497Asp)	rs267606911	0.00001
NM_000257.4(MYH7):c.3634C>T (p.Arg1212Trp)	rs1555337102	0.00001
NM_000257.4(MYH7):c.709C>T (p.Arg237Trp)	rs45516091	0.00001
NM_000257.4(MYH7):c.1106G>A (p.Arg369Gln)	rs397516089
NM_000257.4(MYH7):c.1311C>A (p.Asn437Lys)	rs1595086845
NM_000257.4(MYH7):c.1405G>T (p.Asp469Tyr)	rs397516106
NM_000257.4(MYH7):c.1423C>A (p.Gln475Lys)	rs1566534775
NM_000257.4(MYH7):c.1559G>T (p.Cys520Phe)	rs1892789510
NM_000257.4(MYH7):c.1573G>A (p.Glu525Lys)	rs606231324
NM_000257.4(MYH7):c.1653G>C (p.Lys551Asn)
NM_000257.4(MYH7):c.1791C>A (p.Asn597Lys)	rs397516122
NM_000257.4(MYH7):c.1858_1859del (p.Leu620fs)	rs1566533919
NM_000257.4(MYH7):c.1998T>A (p.His666Gln)	rs1374980600
NM_000257.4(MYH7):c.2086A>C (p.Asn696His)	rs2138668970
NM_000257.4(MYH7):c.2114G>A (p.Cys705Tyr)	rs1555337916
NM_000257.4(MYH7):c.2171T>A (p.Ile724Asn)	rs397516136
NM_000257.4(MYH7):c.2761G>A (p.Glu921Lys)	rs730880759
NM_000257.4(MYH7):c.2775G>T (p.Arg925Ser)
NM_000257.4(MYH7):c.323G>A (p.Arg108His)	rs730880832
NM_000257.4(MYH7):c.514C>G (p.Gln172Glu)	rs2138683978
NM_000257.4(MYH7):c.5390T>C (p.Leu1797Pro)	rs1114167322
NM_000257.4(MYH7):c.5655+5G>A	rs1595070689
NM_000257.4(MYH7):c.602T>C (p.Ile201Thr)	rs397516258
NM_000257.4(MYH7):c.640-2A>T	rs2138681961
NM_000257.4(MYH7):c.732+1del	rs397516266
NM_000257.4(MYH7):c.815G>C (p.Arg272Thr)	rs1555338578

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