List of variants in gene DMXL2 reported as uncertain significance for Nonsyndromic genetic hearing loss

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001378457.1(DMXL2):c.3949A>G (p.Ile1317Val)	rs148766950	0.00037
NM_001378457.1(DMXL2):c.1339G>A (p.Asp447Asn)	rs149014761	0.00031
NM_001378457.1(DMXL2):c.1687A>G (p.Met563Val)	rs772129232	0.00006
NM_001378457.1(DMXL2):c.7717A>G (p.Ile2573Val)	rs202154593	0.00001
NM_001378457.1(DMXL2):c.3937G>A (p.Glu1313Lys)
NM_001378457.1(DMXL2):c.4982A>G (p.Asn1661Ser)
NM_001378457.1(DMXL2):c.7276G>A (p.Val2426Ile)
NM_001378457.1(DMXL2):c.788G>A (p.Gly263Asp)

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