List of variants in gene combination LOC126807246, PDLIM3 reported as likely benign for Primary dilated cardiomyopathy; Hypertrophic cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_014476.6(PDLIM3):c.375T>C (p.Pro125=)	rs372840074	0.00006
NM_014476.6(PDLIM3):c.331-15G>A	rs771774420	0.00001
NM_014476.6(PDLIM3):c.398+9C>T	rs761820729	0.00001
NM_014476.6(PDLIM3):c.378C>T (p.Phe126=)
NM_014476.6(PDLIM3):c.398+12T>A	rs181339407
NM_014476.6(PDLIM3):c.398+12T>C	rs181339407
NM_014476.6(PDLIM3):c.398+15G>A	rs1259024974
NM_014476.6(PDLIM3):c.398+8G>A	rs1215013585

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