Related gene-specific medical variations for Gene (Select 339231) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315041	NM_001040025.3(ARL16):c.19G>C (p.Ala7Pro)	ARL16, LOC112533681 (A7P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129549	NM_001040025.3(ARL16):c.-3G>A	ARL16, LOC112533681	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3129544	NM_001040025.3(ARL16):c.38C>T (p.Thr13Met)	ARL16, LOC112533681 (T13M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2484957	NM_001040025.3(ARL16):c.8T>C (p.Leu3Pro)	ARL16, LOC112533681 (L3P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2241184	NM_001040025.3(ARL16):c.-20C>A	ARL16, LOC112533681	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 208393	NM_001040025.3(ARL16):c.-41G>T	ARL16, LOC112533681	Single nucleotide variant (5 prime UTR variant +1 more)	Childhood-onset schizophrenia	GLikely pathogenic

ClinVar