"Clinical Genetics, Academic Medical Center"[submitter] AND "ZNF408"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1206255	NM_024741.3(ZNF408):c.52+36G>C	ZNF408 (G8R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 790089	NM_024741.3(ZNF408):c.903G>T (p.Pro301=)	ZNF408	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 713577	NM_024741.3(ZNF408):c.1497G>A (p.Pro499=)	ZNF408	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 933647	NM_024741.3(ZNF408):c.1786C>T (p.Arg596Cys)	ZNF408 (R588C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1160598	NM_024741.3(ZNF408):c.2019T>G (p.Val673=)	ZNF408	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 969022	NM_024741.3(ZNF408):c.2058T>G (p.Phe686Leu)	ZNF408 (F678L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

ClinVar