ClinVar Miner

List of variants in gene SZT2 reported as uncertain significance by New York Genome Center

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001365999.1(SZT2):c.4727G>A (p.Arg1576His) rs143935839 0.00119
NM_001365999.1(SZT2):c.6343C>G (p.Pro2115Ala) rs147309177 0.00073
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.9388C>T (p.Arg3130Trp) rs773708821 0.00011
NM_001365999.1(SZT2):c.6779G>A (p.Arg2260Gln) rs374546223 0.00009
NM_001365999.1(SZT2):c.3187G>T (p.Val1063Leu) rs369627050 0.00008
NM_001365999.1(SZT2):c.7514G>A (p.Arg2505His) rs374896394 0.00006
NM_001365999.1(SZT2):c.3788G>A (p.Arg1263Gln) rs149633993 0.00005
NM_001365999.1(SZT2):c.7582C>T (p.Arg2528Cys) rs139028803 0.00004
NM_001365999.1(SZT2):c.6335C>T (p.Ala2112Val) rs746338306 0.00003
NM_001365999.1(SZT2):c.9941A>G (p.Lys3314Arg) rs758380489 0.00002
NM_001365999.1(SZT2):c.4034C>A (p.Ala1345Glu) rs1026710468 0.00001
NM_001365999.1(SZT2):c.4972T>A (p.Leu1658Ile) rs745970630 0.00001
NM_001365999.1(SZT2):c.9892C>T (p.Arg3298Cys) rs764177776 0.00001
NM_001365999.1(SZT2):c.10262A>G (p.Asn3421Ser) rs1458905925
NM_001365999.1(SZT2):c.1678G>T (p.Ala560Ser) rs1652436805
NM_001365999.1(SZT2):c.3784C>T (p.Pro1262Ser) rs2153933426
NM_001365999.1(SZT2):c.9799C>T (p.Arg3267Trp) rs538720577

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