"Genetic Services Laboratory, University of Chicago"[submitter] AND "T - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1336869	NM_015421.4(TMEM186):c.3+185A>G	PMM2, TMEM186	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 1337239	NM_015421.4(TMEM186):c.3+130A>G	PMM2, TMEM186	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 1336657	NM_015421.4(TMEM186):c.3+67G>A	PMM2, TMEM186	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 1212443	NM_015421.4(TMEM186):c.3+27G>A	PMM2, TMEM186	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1326750	NM_015421.4(TMEM186):c.3+20G>T	PMM2, TMEM186	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 702357	NM_015421.4(TMEM186):c.1A>G (p.Met1Val)	PMM2, TMEM186 (M1V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign/Likely benign

ClinVar