Variants in gene TNFRSF1A 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001065.4(TNFRSF1A):c.36A>G (p.Pro12=)	rs767455	0.39963
NM_001065.4(TNFRSF1A):c.625+10A>G	rs1800693	0.38055
NM_001065.4(TNFRSF1A):c.362G>A (p.Arg121Gln)	rs4149584	0.01206
NM_001065.4(TNFRSF1A):c.1110C>T (p.Arg370=)	rs201683984	0.00236
NM_001065.4(TNFRSF1A):c.645C>T (p.Pro215=)	rs147075345	0.00020
NM_001065.4(TNFRSF1A):c.482A>G (p.Lys161Arg)	rs578112440	0.00001

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