List of variants in gene XPR1 reported as uncertain significance for idiopathic disease

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004736.4(XPR1):c.762C>T (p.Ala254=)	rs776659201	0.00007
NM_004736.4(XPR1):c.2018G>A (p.Arg673His)	rs368909346	0.00005
NM_004736.4(XPR1):c.1954G>A (p.Val652Ile)	rs748681314	0.00001
NM_004736.4(XPR1):c.1158C>G (p.Phe386Leu)	rs61742073
NM_004736.4(XPR1):c.1811G>A (p.Arg604Gln)	rs2102226595
NM_004736.4(XPR1):c.66T>C (p.Tyr22=)

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