FAM3B[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 714834	NM_058186.4(FAM3B):c.48C>T (p.Phe16=)	FAM3B	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 769132	NM_058186.4(FAM3B):c.123C>G (p.Ala41=)	FAM3B	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 710984	NM_058186.4(FAM3B):c.163+10G>A	FAM3B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2515355	NM_058186.4(FAM3B):c.185A>G (p.Lys62Arg)	FAM3B (K14R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277421	NM_058186.4(FAM3B):c.566T>C (p.Val189Ala)	FAM3B (V189A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277420	NM_058186.4(FAM3B):c.584G>T (p.Gly195Val)	FAM3B (G147V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204299	NM_058186.4(FAM3B):c.619A>T (p.Ile207Phe)	FAM3B (I207F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar