ClinVar Miner

List of variants reported as likely benign for Knobloch syndrome 1 by 3billion

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001379500.1(COL18A1):c.107-12513C>T	rs375087150	0.00005
NM_001379500.1(COL18A1):c.1221G>A (p.Pro407=)	rs368902481	0.00004
NC_000021.9:g.45405398C>T	rs754075778	0.00002

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