ClinVar Miner

List of variants in gene SZT2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001365999.1(SZT2):c.4342C>T (p.Arg1448Cys) rs140004653 0.00061
NM_001365999.1(SZT2):c.8944C>T (p.His2982Tyr) rs754779853 0.00045
NM_001365999.1(SZT2):c.6185G>A (p.Arg2062Gln) rs200443293 0.00038
NM_001365999.1(SZT2):c.4963C>T (p.Pro1655Ser) rs144139818 0.00031
NM_001365999.1(SZT2):c.4064A>G (p.His1355Arg) rs149741610 0.00022
NM_001365999.1(SZT2):c.5813T>C (p.Ile1938Thr) rs139028174 0.00017
NM_001365999.1(SZT2):c.653C>T (p.Ser218Leu) rs376862612 0.00013
NM_001365999.1(SZT2):c.4892C>T (p.Thr1631Met) rs201312287 0.00009
NM_001365999.1(SZT2):c.5906G>A (p.Arg1969Gln) rs201099906 0.00004
NM_001365999.1(SZT2):c.9880C>T (p.Arg3294Trp) rs199787819 0.00004
NM_001365999.1(SZT2):c.3511G>T (p.Gly1171Trp) rs201767217 0.00003
NM_001365999.1(SZT2):c.2353A>G (p.Ser785Gly) rs754599484 0.00001
NM_001365999.1(SZT2):c.5316A>G (p.Glu1772=) rs797046032 0.00001
NM_001365999.1(SZT2):c.9731C>T (p.Pro3244Leu) rs774448705 0.00001
NM_001365999.1(SZT2):c.3019A>T (p.Met1007Leu) rs2153933173

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