TMEM18[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2361378	NM_152834.4(TMEM18):c.337G>A (p.Val113Ile)	TMEM18 (V100I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388589	NM_152834.4(TMEM18):c.259G>A (p.Asp87Asn)	TMEM18 (D90N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400369	NM_152834.4(TMEM18):c.215C>T (p.Ala72Val)	TMEM18 (A59V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2309384	NM_152834.4(TMEM18):c.209A>G (p.Asn70Ser)	TMEM18 (N70S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 723817	NM_152834.4(TMEM18):c.179-6T>C	TMEM18	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3179007	NM_152834.4(TMEM18):c.86T>A (p.Met29Lys)	TMEM18 (M32K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268214	NM_152834.4(TMEM18):c.4C>G (p.Pro2Ala)	TMEM18 (P2A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 394319	GRCh37/hg19 2p25.3(chr2:386460-768496)x3	TMEM18	Copy number gain	See cases	GLikely benign

ClinVar