ClinVar Miner

List of variants in gene LYZ reported as uncertain significance for amyloidosis

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_000239.3(LYZ):c.*242C>A rs576522577 0.00113
NM_000239.3(LYZ):c.*608T>C rs192668989 0.00056
NM_000239.3(LYZ):c.*300C>T rs919388445 0.00041
NM_000239.3(LYZ):c.*330C>T rs886049805 0.00007
NM_000239.3(LYZ):c.*426C>T rs980457915 0.00006
NM_000239.3(LYZ):c.*565G>T rs886049808 0.00006
NM_000239.3(LYZ):c.*331G>A rs762377090 0.00004
NM_000239.3(LYZ):c.*442T>G rs886049807 0.00004
NM_000239.3(LYZ):c.*866C>T rs959564680 0.00004
NM_000239.3(LYZ):c.175C>T (p.Arg59Ter) rs374990260 0.00004
NM_000239.3(LYZ):c.*544C>T rs961590974 0.00003
NM_000239.3(LYZ):c.269G>A (p.Gly90Glu) rs141911537 0.00003
NM_000239.3(LYZ):c.*221C>T rs886049804 0.00002
NM_000239.3(LYZ):c.151A>T (p.Lys51Ter) rs367682582 0.00002
NM_000239.3(LYZ):c.*470C>T rs554855169 0.00001
NM_000239.3(LYZ):c.*891G>A rs1874912403 0.00001
NM_000239.3(LYZ):c.199G>C (p.Asp67His) rs387906535 0.00001
NM_000239.3(LYZ):c.*122A>G rs1874886327
NM_000239.3(LYZ):c.*266G>C rs188313797
NM_000239.3(LYZ):c.*280_*289dup rs71094709
NM_000239.3(LYZ):c.*289_*290insTTTTTTTTTTTTT rs71094709
NM_000239.3(LYZ):c.*309G>A rs982245735
NM_000239.3(LYZ):c.*404G>T rs1874896191
NM_000239.3(LYZ):c.*440T>A rs886049806
NM_000239.3(LYZ):c.*565G>A rs886049808
NM_000239.3(LYZ):c.*771A>G rs1874909219
NM_000239.3(LYZ):c.*814C>A rs886049810
NM_000239.3(LYZ):c.107A>G (p.Asp36Gly)
NM_000239.3(LYZ):c.10C>T (p.Leu4Phe)
NM_000239.3(LYZ):c.156G>T (p.Trp52Cys)
NM_000239.3(LYZ):c.176G>A (p.Arg59Gln)
NM_000239.3(LYZ):c.209C>G (p.Thr70Ser) rs1349579951
NM_000239.3(LYZ):c.228G>A (p.Gln76=)
NM_000239.3(LYZ):c.230T>C (p.Ile77Thr)
NM_000239.3(LYZ):c.238C>T (p.Arg80Cys)
NM_000239.3(LYZ):c.281C>G (p.Ala94Gly)
NM_000239.3(LYZ):c.302-7_302-5dup
NM_000239.3(LYZ):c.322G>A (p.Ala108Thr)
NM_000239.3(LYZ):c.381-1G>A
NM_000239.3(LYZ):c.381-2A>T
NM_000239.3(LYZ):c.416T>C (p.Val139Ala)
NM_000239.3(LYZ):c.442G>A (p.Val148Met)
NM_000239.3(LYZ):c.44_45delinsTT (p.Thr15Ile)
NM_000239.3(LYZ):c.5A>G (p.Lys2Arg)
NM_000239.3(LYZ):c.86del (p.Thr29fs) rs1565669113

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