List of variants in gene combination LOC126807246, PDLIM3 reported as benign for not specified

Minimum submission review status:		Collection method:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_014476.6(PDLIM3):c.379G>A (p.Val127Met)	rs11944325	0.02959
NM_014476.6(PDLIM3):c.331-354G>A	rs28447263	0.02537
NM_014476.6(PDLIM3):c.387G>A (p.Pro129=)	rs138670107	0.00111
NM_014476.6(PDLIM3):c.331-16C>T	rs200663921	0.00027

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