List of variants in gene EFEMP2 reported as uncertain significance for Cutis Laxa, Recessive

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016938.4(EFEMP2):c.-229G>C	rs886048510	0.00036
NM_016938.4(EFEMP2):c.-143_-140GGCG[4]	rs886048508
NM_016938.4(EFEMP2):c.-181G>A	rs886048509

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