ClinVar Miner

List of variants in gene LYZ studied for amyloidosis

Included ClinVar conditions (39):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_000239.3(LYZ):c.*178C>T rs710794 0.89111
NM_000239.3(LYZ):c.*835C>T rs1384 0.40016
NM_000239.3(LYZ):c.*655G>T rs8612 0.10799
NM_000239.3(LYZ):c.-1C>T rs513342 0.06603
NM_000239.3(LYZ):c.263C>A (p.Thr88Asn) rs1800973 0.04360
NM_000239.3(LYZ):c.*461G>A rs531233279 0.00770
NM_000239.3(LYZ):c.10C>G (p.Leu4Val) rs58131341 0.00302
NM_000239.3(LYZ):c.*890T>C rs188271229 0.00204
NM_000239.3(LYZ):c.*418C>A rs534565279 0.00177
NM_000239.3(LYZ):c.*415G>A rs183441118 0.00159
NM_000239.3(LYZ):c.*413G>T rs193040437 0.00128
NM_000239.3(LYZ):c.*169G>A rs568058282 0.00126
NM_000239.3(LYZ):c.*242C>A rs576522577 0.00113
NM_000239.3(LYZ):c.*191A>G rs183375295 0.00101
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.*442T>G rs886049807 0.00004
NM_000239.3(LYZ):c.*866C>T rs959564680 0.00004
NM_000239.3(LYZ):c.156G>A (p.Trp52Ter) rs764263034 0.00004
NM_000239.3(LYZ):c.175C>T (p.Arg59Ter) rs374990260 0.00004
NM_000239.3(LYZ):c.434G>A (p.Gly145Asp) rs762616173 0.00004
NM_000239.3(LYZ):c.*331G>A rs762377090 0.00003
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.272C>G (p.Ala91Gly) rs776898103 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>A rs188313797
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.*521G>A rs567541896
NM_000239.3(LYZ):c.*565G>A rs886049808
NM_000239.3(LYZ):c.*735del rs148802204
NM_000239.3(LYZ):c.*771A>G rs1874909219
NM_000239.3(LYZ):c.*814C>A rs886049810
NM_000239.3(LYZ):c.209C>G (p.Thr70Ser) rs1349579951
NM_000239.3(LYZ):c.221T>C (p.Ile74Thr) rs121913547
NM_000239.3(LYZ):c.223T>A (p.Phe75Ile) rs121913549
NM_000239.3(LYZ):c.244T>A (p.Trp82Arg) rs387906536
NM_000239.3(LYZ):c.244T>C (p.Trp82Arg) rs387906536
NM_000239.3(LYZ):c.415G>C (p.Val139Leu) rs367623154
NM_000239.3(LYZ):c.86del (p.Thr29fs) rs1565669113

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