Variants in gene SETX with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.2975A>G (p.Lys992Arg)	rs61742937	0.01445
NM_015046.7(SETX):c.2672T>C (p.Val891Ala)	rs148181729	0.00470
NM_015046.7(SETX):c.7724C>T (p.Pro2575Leu)	rs34000644	0.00304
NM_015046.7(SETX):c.3010A>G (p.Asn1004Asp)	rs77984885	0.00075
NM_015046.7(SETX):c.3826C>G (p.Gln1276Glu)	rs148604312	0.00039
NM_015046.7(SETX):c.7432A>G (p.Thr2478Ala)	rs142303658	0.00038
NM_015046.7(SETX):c.4433C>A (p.Ala1478Glu)	rs143661911	0.00034
NM_015046.7(SETX):c.1869A>C (p.Glu623Asp)	rs139200312	0.00015
NM_015046.7(SETX):c.7490G>A (p.Ser2497Asn)	rs61735488	0.00013
NM_015046.7(SETX):c.3016G>A (p.Gly1006Arg)	rs141266068	0.00006
NM_015046.7(SETX):c.4225A>T (p.Asn1409Tyr)	rs373375060	0.00005
NM_015046.7(SETX):c.4865C>T (p.Pro1622Leu)	rs140781535	0.00005
NM_015046.7(SETX):c.3968G>A (p.Arg1323Gln)	rs369542231	0.00004
NM_015046.7(SETX):c.4828C>T (p.Leu1610Phe)	rs749891883	0.00004
NM_015046.7(SETX):c.3057TGA[5] (p.Asp1024del)	rs572772837

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