ClinVar Miner

List of variants in gene TRIM37 reported as benign by CeGaT Center for Human Genetics Tuebingen

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015294.6(TRIM37):c.1748C>A (p.Pro583His)	rs147363016	0.00368
NM_015294.6(TRIM37):c.398C>T (p.Ala133Val)	rs61758100

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