ClinVar Miner

List of variants in gene HGF reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_000601.6(HGF):c.137C>T (p.Ala46Val) rs150267054 0.00139
NM_000601.6(HGF):c.885C>T (p.Asp295=) rs141751290 0.00028
NM_000601.6(HGF):c.471A>G (p.Pro157=) rs142045938 0.00015
NM_000601.6(HGF):c.258T>C (p.Ala86=) rs370202240 0.00010
NM_000601.6(HGF):c.270T>C (p.Asp90=) rs145598174 0.00009
NM_000601.6(HGF):c.1832G>C (p.Ser611Thr) rs141774517 0.00007
NM_000601.6(HGF):c.1814C>T (p.Thr605Ile) rs147075806 0.00006
NM_000601.6(HGF):c.865+11G>A rs761252474 0.00005
NM_000601.6(HGF):c.2179C>T (p.Gln727Ter) rs140790665 0.00004
NM_000601.6(HGF):c.1818T>C (p.Ile606=) rs762445545 0.00002
NM_000601.6(HGF):c.1041-12T>C rs546227025

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