ClinVar Miner

List of variants reported as uncertain significance for 3M syndrome 2 by Revvity Omics, Revvity

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015311.3(OBSL1):c.4133C>T (p.Thr1378Met)	rs200449388	0.00009
NM_015311.3(OBSL1):c.3994C>T (p.Arg1332Trp)	rs200837976	0.00004
NM_015311.3(OBSL1):c.3892G>A (p.Gly1298Ser)

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