ClinVar Miner

List of variants reported as likely benign by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
UGT1A1*6	rs4148323	0.01140
NM_001267550.2(TTN):c.92176C>T (p.Pro30726Ser)	rs72648247	0.00184
NM_001256071.3(RNF213):c.8833C>T (p.Arg2945Cys)	rs540094757	0.00002

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