ClinVar Miner

List of variants in gene LZTR1 reported as uncertain significance for canthal anomaly

Included ClinVar conditions (57):
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Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_006767.4(LZTR1):c.1055A>C (p.Tyr352Ser)
NM_006767.4(LZTR1):c.1234C>T (p.Arg412Cys) rs747430075
NM_006767.4(LZTR1):c.1254G>C (p.Arg418Ser)
NM_006767.4(LZTR1):c.1254G>T (p.Arg418Ser)
NM_006767.4(LZTR1):c.1382C>A (p.Ala461Asp) rs1569156890
NM_006767.4(LZTR1):c.1385T>C (p.Ile462Thr) rs147684991
NM_006767.4(LZTR1):c.1585T>C (p.Tyr529His) rs767374538
NM_006767.4(LZTR1):c.1739T>C (p.Leu580Pro) rs1555928697
NM_006767.4(LZTR1):c.1943-256C>T rs761685529
NM_006767.4(LZTR1):c.1982G>A (p.Gly661Glu) rs750582696
NM_006767.4(LZTR1):c.2070-12C>A
NM_006767.4(LZTR1):c.2173C>T (p.Arg725Cys)
NM_006767.4(LZTR1):c.2245T>C (p.Tyr749His) rs1601723615
NM_006767.4(LZTR1):c.2246A>G (p.Tyr749Cys) rs755260815
NM_006767.4(LZTR1):c.2437A>C (p.Ser813Arg)
NM_006767.4(LZTR1):c.2462T>C (p.Ile821Thr) rs1275511136
NM_006767.4(LZTR1):c.2509G>A (p.Gly837Ser)
NM_006767.4(LZTR1):c.271A>G (p.Met91Val) rs1135401945
NM_006767.4(LZTR1):c.272T>C (p.Met91Thr) rs1555927321
NM_006767.4(LZTR1):c.322G>A (p.Ala108Thr)
NM_006767.4(LZTR1):c.360C>A (p.His120Gln) rs1249605552
NM_006767.4(LZTR1):c.58G>A (p.Ala20Thr)
NM_006767.4(LZTR1):c.594-3C>T
NM_006767.4(LZTR1):c.842C>T (p.Pro281Leu) rs1390048261

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