List of variants in gene TRIM37 reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

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_015294.6(TRIM37):c.2136C>T (p.Ser712=)	rs768860943	0.00006
NM_015294.6(TRIM37):c.2169A>G (p.Ala723=)	rs771713259	0.00006
NM_015294.6(TRIM37):c.2229A>G (p.Ser743=)	rs1555650856
NM_015294.6(TRIM37):c.810-13dup	rs367700401

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