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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_173630.4(RTTN):c.2990C>T (p.Ala997Val)	rs143471549	0.00255
NM_173630.4(RTTN):c.3338G>A (p.Cys1113Tyr)	rs117774280	0.00217
NM_173630.4(RTTN):c.5212C>T (p.His1738Tyr)	rs35068710	0.00210
NM_173630.4(RTTN):c.5883G>A (p.Leu1961=)	rs35313369	0.00185
NM_173630.4(RTTN):c.3048G>A (p.Pro1016=)	rs149233888	0.00176
NM_173630.4(RTTN):c.1221A>G (p.Glu407=)	rs112327299	0.00081

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