ClinVar Miner

List of variants in gene DMXL2 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001378457.1(DMXL2):c.2096T>C (p.Ile699Thr)	rs117017152	0.00040
NM_001378457.1(DMXL2):c.4966T>G (p.Ser1656Ala)	rs748052252	0.00004

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