List of variants in gene TRIM37 reported 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
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_015294.6(TRIM37):c.493-2A>G	rs186251998	0.00065
NM_015294.6(TRIM37):c.2240A>G (p.Asn747Ser)	rs143613788	0.00053
NM_015294.6(TRIM37):c.296A>G (p.His99Arg)	rs143241826	0.00008
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.1189G>A (p.Val397Met)	rs148604776	0.00003
NM_015294.6(TRIM37):c.2600T>C (p.Leu867Pro)	rs1298434776	0.00001
NM_015294.6(TRIM37):c.2229A>G (p.Ser743=)	rs1555650856
NM_015294.6(TRIM37):c.810-13dup	rs367700401
NM_015294.6(TRIM37):c.810-3del	rs367700401

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