ClinVar Miner

List of variants in gene LZTR1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.651+84A>G rs5752397 0.02904
NM_006767.4(LZTR1):c.1150-54G>A rs5761738 0.02016
NM_006767.4(LZTR1):c.792-304G>C rs117710462 0.01931
NM_006767.4(LZTR1):c.791+186C>T rs58324299 0.01914
NM_006767.4(LZTR1):c.1260+156G>A rs739521 0.01757
NM_006767.4(LZTR1):c.1942+165A>G rs5761754 0.01683
NM_006767.4(LZTR1):c.1260+217G>T rs739522 0.01675
NM_006767.4(LZTR1):c.1353+58G>A rs2329636 0.01662
NM_006767.4(LZTR1):c.*182G>A rs117248731 0.01654
NM_006767.4(LZTR1):c.*171A>C rs113894701 0.01558
NM_006767.4(LZTR1):c.1942+295G>T rs75663780 0.01483
NM_006767.4(LZTR1):c.791+138C>T rs77604252 0.01403
NM_006767.4(LZTR1):c.593+186G>A rs111871065 0.01192
NM_006767.4(LZTR1):c.264-247A>G rs114940264 0.01038
NM_006767.4(LZTR1):c.651+227A>G rs114382769 0.01005
NM_006767.4(LZTR1):c.1260+208G>A rs75405655 0.00995
NM_006767.4(LZTR1):c.791+34C>T rs148414532 0.00973
NM_006767.4(LZTR1):c.321-106A>G rs59283742 0.00856
NM_006767.4(LZTR1):c.791+153C>T rs118059952 0.00791
NM_006767.4(LZTR1):c.510-234G>C rs114061234 0.00771
NM_006767.4(LZTR1):c.201-40A>G rs187245425 0.00732
NM_006767.4(LZTR1):c.791+277C>T rs113835435 0.00598
NM_006767.4(LZTR1):c.652-202G>A rs74902115 0.00573
NM_006767.4(LZTR1):c.1150-35C>T rs73879466 0.00541
NM_006767.4(LZTR1):c.201-8C>T rs183476594 0.00520
NM_006767.4(LZTR1):c.993+179A>C rs112884416 0.00442
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.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.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.1164G>A (p.Arg388=) rs200801199 0.00040
NM_006767.4(LZTR1):c.2511C>T (p.Gly837=) rs202072955 0.00036
NM_006767.4(LZTR1):c.678A>T (p.Pro226=) rs200001328 0.00021
NM_006767.4(LZTR1):c.1329C>T (p.Cys443=) rs145473401 0.00016
NM_006767.4(LZTR1):c.945C>T (p.Asp315=) rs559942119 0.00016
NM_006767.4(LZTR1):c.1194C>T (p.Asp398=) rs557960320 0.00015
NM_006767.4(LZTR1):c.594-3C>T rs373968693 0.00015
NM_006767.4(LZTR1):c.2247C>T (p.Tyr749=) rs779077819 0.00004
NM_006767.4(LZTR1):c.2355A>G (p.Ala785=) rs751681487 0.00004
NM_006767.4(LZTR1):c.1354-19T>C rs376603441 0.00003
NM_006767.4(LZTR1):c.1615+4C>T rs551144605 0.00002
NM_006767.4(LZTR1):c.2070-12C>T rs779677120 0.00001
NM_006767.4(LZTR1):c.2295G>A (p.Glu765=) rs1175579360 0.00001
NM_006767.4(LZTR1):c.375C>A (p.Val125=) rs201356174 0.00001
NM_006767.4(LZTR1):c.990C>T (p.Ser330=) rs548900356 0.00001
NM_006767.4(LZTR1):c.*20A>T rs73394511
NM_006767.4(LZTR1):c.*75T>C rs549934273
NM_006767.4(LZTR1):c.*77C>G rs116921548
NM_006767.4(LZTR1):c.1620T>C (p.His540=) rs141610191
NM_006767.4(LZTR1):c.1818C>T (p.Ser606=)
NM_006767.4(LZTR1):c.2220-206_2220-199del
NM_006767.4(LZTR1):c.320+13G>T rs188924002
NM_006767.4(LZTR1):c.320+15G>A rs1042833679
NM_006767.4(LZTR1):c.321-102_321-101dup rs58365624
NM_006767.4(LZTR1):c.510-4C>G rs1413440011
NM_006767.4(LZTR1):c.651+10_651+46del rs541944601
NM_006767.4(LZTR1):c.652-265del rs563744807

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