List of variants in gene SZT2 reported as likely pathogenic by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001365999.1(SZT2):c.5088+2T>C	rs552956642	0.00001
NM_001365999.1(SZT2):c.1108_1111del (p.Phe370fs)	rs2545801238
NM_001365999.1(SZT2):c.4401+1G>A	rs2545825608
NM_001365999.1(SZT2):c.7488dup (p.Asp2497fs)	rs2545850014

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