List of variants reported as likely benign for Cutis laxa, autosomal recessive, type 1B by Illumina Laboratory Services, Illumina

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016938.5(EFEMP2):c.138C>T (p.Asp46=)	rs2234457	0.00375
NM_016938.5(EFEMP2):c.368-11G>A	rs181514768	0.00272
NM_016938.5(EFEMP2):c.368-4G>A	rs111550973	0.00223
NM_016938.5(EFEMP2):c.139C>T (p.Pro47Ser)	rs144320036	0.00104

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