List of variants in gene LAMA4 studied for hypertrophic cardiomyopathy

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys)	rs138153075	0.00135
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His)	rs3752579	0.00093
NM_001105206.3(LAMA4):c.2614C>G (p.Pro872Ala)	rs180931319	0.00028
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr)	rs141261442	0.00022
NM_001105206.3(LAMA4):c.1277T>C (p.Met426Thr)	rs200112094	0.00013
NM_001105206.3(LAMA4):c.2189G>A (p.Arg730His)	rs781825990	0.00008
NM_001105206.3(LAMA4):c.3043G>C (p.Val1015Leu)	rs730880122	0.00004
NM_001105206.3(LAMA4):c.3563T>G (p.Leu1188Arg)	rs782291756	0.00004
NM_001105206.3(LAMA4):c.105C>G (p.Asp35Glu)	rs572035776	0.00002
NM_001105206.3(LAMA4):c.814+7A>C	rs730880124	0.00001

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