C1858028[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 749103	NM_001008388.5(CISD2):c.60G>C (p.Arg20=)	CISD2, LOC129992892	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1513999	NM_001008388.5(CISD2):c.83C>T (p.Thr28Ile)	CISD2, LOC129992892 (T28I)	Single nucleotide variant (missense variant)	Wolfram syndrome 2 +1 more	GUncertain significance
Select item 1349559	NM_001008388.5(CISD2):c.103+6C>A	CISD2, LOC129992892	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 716908	NM_001008388.5(CISD2):c.104-9C>A	CISD2, SLC9B1	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +2 more	GBenign/Likely benign
Select item 1448359	NM_001008388.5(CISD2):c.239C>T (p.Pro80Leu)	CISD2, SLC9B1 (P80L)	Single nucleotide variant (missense variant +1 more)	Wolfram syndrome 2 +1 more	GUncertain significance
Select item 136775	NM_001008388.5(CISD2):c.240G>A (p.Pro80=)	SLC9B1, CISD2	Single nucleotide variant (synonymous variant +1 more)	Wolfram syndrome 2 +1 more	GBenign/Likely benign
Select item 508006	NM_001008388.5(CISD2):c.319-20T>C	CISD2, SLC9B1	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign

ClinVar