ClinVar Miner

Variants in gene SZT2 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: 4
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HGVS dbSNP
NM_001365999.1(SZT2):c.4898C>T (p.Ser1633Leu) rs138762270
NM_001365999.1(SZT2):c.5345C>T (p.Ala1782Val) rs138028425
NM_001365999.1(SZT2):c.6335C>T (p.Ala2112Val) rs746338306
NM_001365999.1(SZT2):c.8702C>T (p.Pro2901Leu) rs139027171

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