Variants in gene NEXMIF with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.133G>A (p.Ala45Thr)	rs199960807	0.00030
NM_001008537.3(NEXMIF):c.3775G>A (p.Ala1259Thr)	rs761368099	0.00022
NM_001008537.3(NEXMIF):c.206C>T (p.Ser69Phe)	rs201351157	0.00014
NM_001008537.3(NEXMIF):c.2951A>G (p.Asn984Ser)	rs375623451	0.00013
NM_001008537.3(NEXMIF):c.3402C>A (p.His1134Gln)	rs138632224	0.00011
NM_001008537.3(NEXMIF):c.2672A>G (p.Asn891Ser)	rs186535459	0.00008
NM_001008537.3(NEXMIF):c.3386T>G (p.Phe1129Cys)	rs202207238	0.00006
NM_001008537.3(NEXMIF):c.2130G>A (p.Lys710=)	rs749479992	0.00004
NM_001008537.3(NEXMIF):c.262G>A (p.Glu88Lys)	rs927047621	0.00004
NM_001008537.3(NEXMIF):c.1154G>A (p.Gly385Asp)	rs375109305	0.00002
NM_001008537.3(NEXMIF):c.1418C>T (p.Ser473Phe)	rs1305966854	0.00002
NM_001008537.3(NEXMIF):c.1883G>A (p.Arg628Gln)	rs747436946	0.00002
NM_001008537.3(NEXMIF):c.3319G>A (p.Asp1107Asn)	rs751468762	0.00002
NM_001008537.3(NEXMIF):c.419T>C (p.Met140Thr)	rs766172626	0.00002
NM_001008537.3(NEXMIF):c.1757G>C (p.Gly586Ala)	rs776845564	0.00001
NM_001008537.3(NEXMIF):c.2895A>G (p.Gln965=)	rs1556016407
NM_001008537.3(NEXMIF):c.3347G>C (p.Cys1116Ser)	rs2080102020
NM_001008537.3(NEXMIF):c.3728G>A (p.Arg1243His)	rs1256402686
NM_001008537.3(NEXMIF):c.431G>A (p.Arg144Gln)	rs1029069870

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