ClinVar Miner

List of variants in gene combination LOC130067016, LZTR1 reported as likely benign for Hereditary cancer-predisposing syndrome; Cardiovascular phenotype

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.-4C>T rs573275770 0.00019
NM_006767.4(LZTR1):c.54C>G (p.Gly18=) rs371007598 0.00015
NM_006767.4(LZTR1):c.96T>C (p.His32=) rs372440263 0.00015
NM_006767.4(LZTR1):c.27G>A (p.Gly9=) rs750714248 0.00003
NM_006767.4(LZTR1):c.36G>A (p.Gly12=) rs756364667 0.00001
NM_006767.4(LZTR1):c.102C>T (p.Cys34=)
NM_006767.4(LZTR1):c.108C>T (p.Asp36=)
NM_006767.4(LZTR1):c.12G>A (p.Pro4=)
NM_006767.4(LZTR1):c.21G>C (p.Thr7=)
NM_006767.4(LZTR1):c.21G>T (p.Thr7=)
NM_006767.4(LZTR1):c.22G>T (p.Gly8Trp) rs575193991
NM_006767.4(LZTR1):c.24G>C (p.Gly8=)
NM_006767.4(LZTR1):c.33C>T (p.Ile11=)
NM_006767.4(LZTR1):c.42G>A (p.Ala14=) rs1446469999
NM_006767.4(LZTR1):c.42G>C (p.Ala14=) rs1446469999
NM_006767.4(LZTR1):c.45C>T (p.Ala15=)
NM_006767.4(LZTR1):c.48G>A (p.Leu16=)
NM_006767.4(LZTR1):c.48G>C (p.Leu16=)
NM_006767.4(LZTR1):c.48G>T (p.Leu16=)
NM_006767.4(LZTR1):c.54C>A (p.Gly18=)
NM_006767.4(LZTR1):c.60G>T (p.Ala20=)
NM_006767.4(LZTR1):c.63G>T (p.Arg21=)
NM_006767.4(LZTR1):c.75C>T (p.Ala25=) rs1924228731
NM_006767.4(LZTR1):c.87C>T (p.Asp29=)

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