Variants in gene TNFRSF1A with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001065.4(TNFRSF1A):c.224C>T (p.Pro75Leu)	rs4149637	0.00574
NM_001065.4(TNFRSF1A):c.1110C>T (p.Arg370=)	rs201683984	0.00236
NM_001065.4(TNFRSF1A):c.935G>A (p.Arg312Lys)	rs200900510	0.00113
NM_001065.4(TNFRSF1A):c.789T>C (p.Thr263=)	rs201290189	0.00069
NM_001065.4(TNFRSF1A):c.1075C>T (p.Leu359=)	rs151344628	0.00050
NM_001065.4(TNFRSF1A):c.987C>T (p.Leu329=)	rs138261783	0.00047
NM_001065.4(TNFRSF1A):c.369C>T (p.Thr123=)	rs104895260	0.00036
NM_001065.4(TNFRSF1A):c.645C>T (p.Pro215=)	rs147075345	0.00020
NM_001065.4(TNFRSF1A):c.1206C>T (p.Ser402=)	rs148334665	0.00018
NM_001065.4(TNFRSF1A):c.249G>A (p.Glu83=)	rs104895265	0.00010
NM_001065.4(TNFRSF1A):c.219A>G (p.Pro73=)	rs1469912868
NM_001065.4(TNFRSF1A):c.714G>A (p.Arg238=)	rs200376188

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