Variants in gene TNFRSF13B with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely 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_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_012452.3(TNFRSF13B):c.568G>C (p.Gly190Arg)	rs150101848	0.00083
NM_012452.3(TNFRSF13B):c.605G>A (p.Arg202His)	rs104894649	0.00076
NM_012452.3(TNFRSF13B):c.126T>C (p.Pro42=)	rs377551435	0.00011
NM_012452.3(TNFRSF13B):c.577T>C (p.Cys193Arg)	rs764125338	0.00009
NM_012452.3(TNFRSF13B):c.593G>A (p.Arg198His)	rs150974807	0.00006

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