ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance for Inborn genetic diseases

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Total variants: 6
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HGVS dbSNP
NM_001376.5(DYNC1H1):c.10241A>G (p.Asn3414Ser) rs1555411393
NM_001376.5(DYNC1H1):c.11989C>T (p.Arg3997Trp) rs1399236395
NM_001376.5(DYNC1H1):c.12211A>G (p.Ile4071Val) rs797044851
NM_001376.5(DYNC1H1):c.13303G>A (p.Val4435Ile) rs767195767
NM_001376.5(DYNC1H1):c.752G>A (p.Arg251His) rs794727634
NM_001376.5(DYNC1H1):c.816A>C (p.Leu272Phe) rs1555407950

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