ClinVar Miner

Variants in gene LZTR1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 57
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.2219+13C>T rs144005025 0.00972
NM_006767.4(LZTR1):c.1209C>T (p.Phe403=) rs145833752 0.00550
NM_006767.4(LZTR1):c.201-8C>T rs183476594 0.00520
NM_006767.4(LZTR1):c.2373C>T (p.His791=) rs148993324 0.00299
NM_006767.4(LZTR1):c.2187C>T (p.Tyr729=) rs117346988 0.00222
NM_006767.4(LZTR1):c.741C>T (p.Ser247=) rs114458679 0.00183
NM_006767.4(LZTR1):c.1530C>T (p.His510=) rs190714197 0.00155
NM_006767.4(LZTR1):c.666C>T (p.Gly222=) rs35767542 0.00122
NM_006767.4(LZTR1):c.1395G>A (p.Ala465=) rs142418387 0.00108
NM_006767.4(LZTR1):c.-11G>A rs370616172 0.00097
NM_006767.4(LZTR1):c.1719C>T (p.Ser573=) rs150897932 0.00097
NM_006767.4(LZTR1):c.906G>A (p.Ala302=) rs143128466 0.00090
NM_006767.4(LZTR1):c.453C>T (p.Asp151=) rs142421078 0.00069
NM_006767.4(LZTR1):c.1353+8C>G rs75959644 0.00065
NM_006767.4(LZTR1):c.543G>A (p.Thr181=) rs151294009 0.00063
NM_006767.4(LZTR1):c.1723G>A (p.Asp575Asn) rs139368531 0.00061
NM_006767.4(LZTR1):c.652-10C>A rs200169897 0.00049
NM_006767.4(LZTR1):c.2316C>T (p.Asn772=) rs140327903 0.00047
NM_006767.4(LZTR1):c.2022C>T (p.Asp674=) rs145303406 0.00044
NM_006767.4(LZTR1):c.855C>T (p.Tyr285=) rs140612093 0.00043
NM_006767.4(LZTR1):c.2511C>T (p.Gly837=) rs202072955 0.00036
NM_006767.4(LZTR1):c.2190C>T (p.Gly730=) rs144092577 0.00034
NM_006767.4(LZTR1):c.2301C>T (p.Asn767=) rs112615858 0.00021
NM_006767.4(LZTR1):c.678A>T (p.Pro226=) rs200001328 0.00021
NM_006767.4(LZTR1):c.945C>T (p.Asp315=) rs559942119 0.00016
NM_006767.4(LZTR1):c.1449+18C>G rs369921461 0.00014
NM_006767.4(LZTR1):c.264-14C>T rs199963374 0.00012
NM_006767.4(LZTR1):c.351C>T (p.Pro117=) rs202066345 0.00012
NM_006767.4(LZTR1):c.2205G>A (p.Pro735=) rs368690209 0.00011
NM_006767.4(LZTR1):c.263+7G>A rs185749722 0.00010
NM_006767.4(LZTR1):c.1377C>T (p.His459=) rs752985853 0.00009
NM_006767.4(LZTR1):c.366G>A (p.Ser122=) rs367767120 0.00009
NM_006767.4(LZTR1):c.1548C>T (p.Ala516=) rs545065457 0.00008
NM_006767.4(LZTR1):c.369C>T (p.Ala123=) rs773126123 0.00008
NM_006767.4(LZTR1):c.2325+17G>A rs570834637 0.00006
NM_006767.4(LZTR1):c.593+11G>A rs200649588 0.00006
NM_006767.4(LZTR1):c.1416G>A (p.Arg472=) rs367740343 0.00005
NM_006767.4(LZTR1):c.2514C>T (p.Ala838=) rs772037780 0.00005
NM_006767.4(LZTR1):c.1260+16G>A rs376876059 0.00004
NM_006767.4(LZTR1):c.1353+16C>T rs143592070 0.00004
NM_006767.4(LZTR1):c.1450-14C>T rs767640622 0.00004
NM_006767.4(LZTR1):c.1943-4C>G rs368391573 0.00004
NM_006767.4(LZTR1):c.2247C>T (p.Tyr749=) rs779077819 0.00004
NM_006767.4(LZTR1):c.2274G>A (p.Ala758=) rs144870586 0.00004
NM_006767.4(LZTR1):c.2355A>G (p.Ala785=) rs751681487 0.00004
NM_006767.4(LZTR1):c.1615+4C>T rs551144605 0.00002
NM_006767.4(LZTR1):c.1749C>T (p.Cys583=) rs758399311 0.00002
NM_006767.4(LZTR1):c.522T>G (p.Ala174=) rs745514794 0.00001
NM_006767.4(LZTR1):c.1449+9C>G rs756813850
NM_006767.4(LZTR1):c.1620T>C (p.His540=) rs141610191
NM_006767.4(LZTR1):c.1785+13_1785+33dup
NM_006767.4(LZTR1):c.1992G>A (p.Ala664=)
NM_006767.4(LZTR1):c.2103C>G (p.Pro701=) rs139080986
NM_006767.4(LZTR1):c.263+7_263+10del rs765081424
NM_006767.4(LZTR1):c.320+13G>A rs188924002
NM_006767.4(LZTR1):c.651+10_651+46del rs541944601
NM_006767.4(LZTR1):c.918G>A (p.Thr306=) rs367738742

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