ClinVar Miner

List of variants in gene SZT2 reported as likely benign by Invitae

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_001365999.1(SZT2):c.1107A>G (p.Leu369=) rs533632273
NM_001365999.1(SZT2):c.1791C>T (p.His597=) rs151110718
NM_001365999.1(SZT2):c.2025G>A (p.Pro675=) rs561698107
NM_001365999.1(SZT2):c.2356C>T (p.Leu786=) rs878855007
NM_001365999.1(SZT2):c.2547T>A (p.Ile849=) rs774483969
NM_001365999.1(SZT2):c.2930-4G>A rs780736141
NM_001365999.1(SZT2):c.3216T>C (p.Gly1072=) rs763882399
NM_001365999.1(SZT2):c.3309+9C>T rs140366288
NM_001365999.1(SZT2):c.3804-9G>A rs138670520
NM_001365999.1(SZT2):c.3924A>G (p.Leu1308=) rs1060504947
NM_001365999.1(SZT2):c.4176C>T (p.Thr1392=) rs373047934
NM_001365999.1(SZT2):c.4481-5A>G rs878855008
NM_001365999.1(SZT2):c.588G>A (p.Lys196=) rs774244334
NM_001365999.1(SZT2):c.6117C>T (p.Asp2039=) rs756197807
NM_001365999.1(SZT2):c.6380A>T (p.Tyr2127Phe) rs149812437
NM_001365999.1(SZT2):c.7275T>C (p.Pro2425=) rs771745066
NM_001365999.1(SZT2):c.7443C>T (p.Thr2481=) rs760714768
NM_001365999.1(SZT2):c.8031G>A (p.Ala2677=) rs138303356
NM_001365999.1(SZT2):c.8998-6del rs536641188

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