C3150739[trait identifier] AND "ARUP Laboratories, Molecular Genetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 440345	NM_052945.4(TNFRSF13C):c.475C>T (p.His159Tyr)	TNFRSF13C (H159Y)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 341877	NM_052945.4(TNFRSF13C):c.317G>A (p.Arg106Gln)	LOC130067574, TNFRSF13C (R106Q)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 2 +3 more	GConflicting classifications of pathogenicity
Select item 487214	NM_052945.4(TNFRSF13C):c.229C>T (p.Leu77=)	LOC130067574, TNFRSF13C	Single nucleotide variant (synonymous variant)	Immunodeficiency, common variable, 4 +1 more	GBenign
Select item 440343	NM_052945.4(TNFRSF13C):c.191G>T (p.Gly64Val)	LOC130067574, TNFRSF13C (G64V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 786787	NM_052945.4(TNFRSF13C):c.102C>T (p.Ala34=)	LOC130067574, TNFRSF13C	Single nucleotide variant (synonymous variant)	TNFRSF13C-related disorder +1 more	GLikely benign
Select item 341883	NM_052945.4(TNFRSF13C):c.62C>G (p.Pro21Arg)	LOC130067574, TNFRSF13C (P21R)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 440344	NM_052945.4(TNFRSF13C):c.60C>T (p.Val20=)	LOC130067574, TNFRSF13C	Single nucleotide variant (synonymous variant)	Immunodeficiency, common variable, 4 +2 more	GConflicting classifications of pathogenicity

ClinVar