List of variants reported as likely pathogenic for Pierson syndrome by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002292.4(LAMB2):c.3109+1G>A	rs888830612	0.00001
NM_002292.4(LAMB2):c.2700_2701del (p.Gly901_Gly902insTer)
NM_002292.4(LAMB2):c.2833C>T (p.Gln945Ter)	rs2107639217
NM_002292.4(LAMB2):c.4882dup (p.Ala1628fs)

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