List of variants in gene XDH reported as benign by Illumina Laboratory Services, Illumina

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: 20

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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.*1477A>G	rs6710015	0.43278
NM_000379.4(XDH):c.*518A>G	rs1042039	0.40737
NM_000379.4(XDH):c.*1516C>T	rs1054889	0.40251
NM_000379.4(XDH):c.*1555G>T	rs6752058	0.26925
NM_000379.4(XDH):c.2211C>T (p.Ile737=)	rs2295475	0.24290
NM_000379.4(XDH):c.3717G>A (p.Glu1239=)	rs207440	0.05236
NM_000379.4(XDH):c.*1081A>G	rs45488100	0.03374
NM_000379.4(XDH):c.*41G>C	rs45593434	0.03354
NM_000379.4(XDH):c.627G>A (p.Glu209=)	rs45575032	0.02778
NM_000379.4(XDH):c.1686+8C>T	rs17395224	0.02225
NM_000379.4(XDH):c.1509C>G (p.Gly503=)	rs45612839	0.01566
NM_000379.4(XDH):c.1329G>A (p.Lys443=)	rs45471294	0.01418
NM_000379.4(XDH):c.3886C>T (p.Arg1296Trp)	rs45564939	0.01229
NM_000379.4(XDH):c.1427+15C>A	rs116569100	0.00186
NM_000379.4(XDH):c.3326A>C (p.Asn1109Thr)	rs45547640	0.00060
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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