List of variants in gene XDH reported as benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000379.4(XDH):c.3030T>C (p.Phe1010=)	rs1884725	0.77423
NM_000379.4(XDH):c.3276+12A>G	rs1366813	0.75380
NM_000379.4(XDH):c.3052-12C>G	rs13415401	0.74590
NM_000379.4(XDH):c.2211C>T (p.Ile737=)	rs2295475	0.24290
NM_000379.4(XDH):c.2107A>G (p.Ile703Val)	rs17011368	0.05740
NM_000379.4(XDH):c.3717G>A (p.Glu1239=)	rs207440	0.05236
NM_000379.4(XDH):c.3886C>T (p.Arg1296Trp)	rs45564939	0.01229
NM_000379.4(XDH):c.1751A>C (p.Asp584Ala)	rs45491693	0.00492
NM_000379.4(XDH):c.3271G>C (p.Val1091Leu)	rs45619033	0.00328
NM_000379.4(XDH):c.670C>T (p.Arg224Trp)	rs147533056	0.00040
NM_000379.4(XDH):c.2794G>A (p.Ala932Thr)	rs141291583	0.00018
NM_000379.4(XDH):c.1990G>A (p.Val664Ile)	rs201301387	0.00005
NM_000379.4(XDH):c.2013G>A (p.Val671=)	rs200635805	0.00005

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