ClinVar Miner

List of variants reported as uncertain significance by Institute of Medical Genetics, Medical University of Vienna

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001009944.3(PKD1):c.11872G>C (p.Ala3958Pro)	rs2091492509
NM_002471.4(MYH6):c.2134C>G (p.Pro712Ala)	rs1891416803
NM_006009.4(TUBA1A):c.680T>A (p.Leu227Gln)	rs2121243965

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