ClinVar Miner

Variants in gene SZT2 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: 27
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HGVS dbSNP
NM_001365999.1(SZT2):c.2550+5G>A rs41270349
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=) rs140831372
NM_001365999.1(SZT2):c.2955C>T (p.Cys985=) rs151189395
NM_001365999.1(SZT2):c.3267C>T (p.Val1089=) rs147008168
NM_001365999.1(SZT2):c.4176C>T (p.Thr1392=) rs373047934
NM_001365999.1(SZT2):c.4531G>A (p.Val1511Ile) rs76675748
NM_001365999.1(SZT2):c.4701G>A (p.Leu1567=) rs111932993
NM_001365999.1(SZT2):c.4898C>T (p.Ser1633Leu) rs138762270
NM_001365999.1(SZT2):c.4983T>C (p.Asp1661=) rs139810154
NM_001365999.1(SZT2):c.5075C>T (p.Thr1692Ile) rs149831634
NM_001365999.1(SZT2):c.5517C>T (p.Arg1839=) rs147753139
NM_001365999.1(SZT2):c.6543A>G (p.Leu2181=) rs112461557
NM_001365999.1(SZT2):c.6573C>T (p.Asp2191=) rs114046098
NM_001365999.1(SZT2):c.675G>A (p.Lys225=) rs564963914
NM_001365999.1(SZT2):c.7149C>T (p.Ala2383=) rs60480887
NM_001365999.1(SZT2):c.7256G>A (p.Arg2419Gln) rs72637949
NM_001365999.1(SZT2):c.7395T>C (p.Ile2465=) rs78858677
NM_001365999.1(SZT2):c.7562T>C (p.Val2521Ala) rs150113647
NM_001365999.1(SZT2):c.7573G>A (p.Val2525Ile) rs139486476
NM_001365999.1(SZT2):c.759G>A (p.Ser253=) rs1889586
NM_001365999.1(SZT2):c.7831C>T (p.Leu2611=) rs140744209
NM_001365999.1(SZT2):c.8020T>C (p.Leu2674=) rs187106999
NM_001365999.1(SZT2):c.8177C>G (p.Thr2726Ser) rs145882968
NM_001365999.1(SZT2):c.9292T>C (p.Leu3098=) rs12089231
NM_001365999.1(SZT2):c.9723G>A (p.Ala3241=) rs146635122
NM_001365999.1(SZT2):c.9782G>A (p.Arg3261Gln) rs190363418
NM_001365999.1(SZT2):c.9883C>T (p.Leu3295=) rs534948696

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