List of variants in gene TMEM43 reported as pathogenic for laminopathy

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024334.3(TMEM43):c.271A>G (p.Ile91Val)	rs144811578	0.00009
NM_024334.3(TMEM43):c.253G>A (p.Glu85Lys)	rs397514044

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