ClinVar Miner

Variants in gene LZTR1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 6
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HGVS dbSNP gnomAD frequency
NM_006767.4(LZTR1):c.2187C>T (p.Tyr729=) rs117346988 0.00222
NM_006767.4(LZTR1):c.1530C>T (p.His510=) rs190714197 0.00155
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.2190C>T (p.Gly730=) rs144092577 0.00034
NM_006767.4(LZTR1):c.2232G>A (p.Ala744=) rs139261473 0.00006

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