ClinVar Miner

List of variants reported as uncertain significance for Fraser syndrome 2 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_207361.6(FREM2):c.6109C>A (p.Leu2037Met)	rs539893834	0.00002
NM_207361.6(FREM2):c.2449A>G (p.Thr817Ala)
NM_207361.6(FREM2):c.5477T>C (p.Val1826Ala)

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