List of variants reported as likely benign by SingHealth Duke-NUS Institute of Precision Medicine

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001985.3(ETFB):c.58-318_58-313dup	rs61361626	0.08041
NM_000277.3(PAH):c.158G>A (p.Arg53His)	rs118092776	0.00091
NM_000436.4(OXCT1):c.173C>T (p.Thr58Met)	rs75134564	0.00053
NM_001875.5(CPS1):c.-4_-3insTTC	rs61509952

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