Related gene-specific medical variations for Gene (Select 3603) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323102	NM_181900.3(STARD5):c.577T>C (p.Phe193Leu)	IL16, LOC126862197 +1 more (F193L)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3285752	NM_172217.5(IL16):c.1456C>A (p.Pro486Thr)	IL16, LOC130057750 (P316T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3285744	NM_172217.5(IL16):c.1450G>A (p.Gly484Arg)	IL16, LOC130057750 (G314R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3170971	NM_181900.3(STARD5):c.513C>G (p.Asn171Lys)	IL16, LOC126862197 +1 more (N171K)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2358031	NM_181900.3(STARD5):c.524T>C (p.Phe175Ser)	IL16, LOC126862197 +1 more (F175S)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2238192	NM_181900.3(STARD5):c.596G>A (p.Arg199Gln)	IL16, LOC126862197 +1 more (R199Q)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 1261119	NM_172217.5(IL16):c.*643T>C	IL16, STARD5	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign

ClinVar