List of variants in gene DDAH2 reported as uncertain significance

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001303007.2(DDAH2):c.454G>C (p.Val152Leu)	rs993493504	0.00001
NM_001303007.2(DDAH2):c.607A>G (p.Thr203Ala)	rs773811465	0.00001
NM_001303007.2(DDAH2):c.806G>T (p.Gly269Val)	rs1323828894	0.00001
NM_001303007.2(DDAH2):c.251A>T (p.Asp84Val)
NM_001303007.2(DDAH2):c.464C>T (p.Thr155Met)	rs150832184
NM_001303007.2(DDAH2):c.614A>G (p.His205Arg)
NM_001303007.2(DDAH2):c.709C>T (p.Arg237Cys)
NM_001303007.2(DDAH2):c.725T>C (p.Leu242Pro)
NM_001303007.2(DDAH2):c.76G>C (p.Gly26Arg)

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