Related gene-specific medical variations for Gene (Select 5777) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3311467	NM_002831.6(PTPN6):c.1674-118G>A	LOC130007304, PTPN6 (V567M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454275	NM_002831.6(PTPN6):c.365C>T (p.Thr122Met)	LOC130007296, PTPN6 (T122M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2429853	NM_002831.6(PTPN6):c.1206+2T>G	PTPN6	Single nucleotide variant (splice donor variant)	Autism spectrum disorder	GUncertain significance
Select item 2290839	NM_002831.6(PTPN6):c.1331C>A (p.Pro444His)	LOC130007299, PTPN6 (P444H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234583	NM_002831.6(PTPN6):c.1674-132C>A	LOC130007304, PTPN6 (S562Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 725610	NM_002831.6(PTPN6):c.1674-110G>A	LOC130007304, PTPN6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

ClinVar