ClinVar Miner

List of variants reported as uncertain significance for Brain small vessel disease 1 with or without ocular anomalies by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001845.6(COL4A1):c.7C>A (p.Pro3Thr)	rs751749989	0.00048
NM_001845.6(COL4A1):c.144+1G>A	rs2139245731
NM_001845.6(COL4A1):c.2627-1G>A	rs1064796811
NM_001845.6(COL4A1):c.3556+4A>G

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