ClinVar Miner

List of variants in gene SETD2 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014159.7(SETD2):c.3851A>T (p.His1284Leu)	rs976218064	0.00001
NM_014159.7(SETD2):c.1246A>G (p.Asn416Asp)
NM_014159.7(SETD2):c.4481T>C (p.Ile1494Thr)

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