List of variants in gene XDH reported as uncertain significance by GeneDx

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)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000379.4(XDH):c.3536T>C (p.Ile1179Thr)	rs139515054	0.00218
NM_000379.4(XDH):c.1868C>T (p.Thr623Ile)	rs45448694	0.00137
NM_000379.4(XDH):c.1686+1G>C	rs148412639	0.00057
NM_000379.4(XDH):c.1597G>A (p.Glu533Lys)	rs147476468	0.00015
NM_000379.4(XDH):c.2698C>T (p.Arg900Trp)	rs763704314	0.00003
NM_000379.4(XDH):c.1630G>A (p.Ala544Thr)	rs750230700	0.00001
NM_000379.4(XDH):c.706T>A (p.Trp236Arg)	rs2465401886
NM_000379.4(XDH):c.880C>G (p.Pro294Ala)	rs1408082938

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