ClinVar Miner

List of variants reported as likely pathogenic for Nephrotic syndrome, type 3 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_016341.4(PLCE1):c.4483C>T (p.Arg1495Ter)	rs548655036	0.00001
NM_016341.4(PLCE1):c.1809+1G>C
NM_016341.4(PLCE1):c.3260del (p.Lys1087fs)

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