List of variants in gene combination ASTN2, TRIM32 reported as likely pathogenic by Eurofins Ntd Llc (ga)

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.1108del (p.Met370fs)	rs759376012
NM_012210.4(TRIM32):c.116_122del (p.Cys39fs)	rs1554732594
NM_012210.4(TRIM32):c.1569_1575del (p.Glu524fs)	rs886044106

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