List of variants in gene MYOC reported by OMIM

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000261.2(MYOC):c.1102C>T (p.Gln368Ter)	rs74315329	0.00089
NM_000261.2(MYOC):c.136C>T (p.Arg46Ter)	rs74315337	0.00024
NM_000261.2(MYOC):c.1196G>T (p.Gly399Val)	rs28936694	0.00002
NM_000261.2(MYOC):c.144G>T (p.Gln48His)	rs74315339	0.00001
NM_000261.2(MYOC):c.1010A>G (p.Gln337Arg)	rs74315335
NM_000261.2(MYOC):c.1091G>T (p.Gly364Val)	rs121909193
NM_000261.2(MYOC):c.1099G>A (p.Gly367Arg)	rs74315334
NM_000261.2(MYOC):c.1109C>T (p.Pro370Leu)	rs74315330
NM_000261.2(MYOC):c.1138G>C (p.Asp380His)	rs121909194
NM_000261.2(MYOC):c.1267A>G (p.Lys423Glu)	rs74315336
NM_000261.2(MYOC):c.1297T>C (p.Cys433Arg)	rs74315338
NM_000261.2(MYOC):c.1309T>C (p.Tyr437His)	rs74315328
NM_000261.2(MYOC):c.1430T>A (p.Ile477Asn)	rs74315331
NM_000261.2(MYOC):c.1430T>G (p.Ile477Ser)	rs74315331
NM_000261.2(MYOC):c.1440C>A (p.Asn480Lys)	rs74315332
NM_000261.2(MYOC):c.734G>A (p.Cys245Tyr)	rs74315340
NM_000261.2(MYOC):c.754G>A (p.Gly252Arg)	rs74315341

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