ClinVar for PubMed (Select 12694232) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1071369	NC_000002.11:g.(?_47630252)_(47635714_?)del	MSH2	Deletion	Hereditary nonpolyposis colorectal neoplasms	GPathogenic
Select item 1071368	NC_000002.11:g.(?_47630150)_(47635704_?)del	MSH2	Deletion	Hereditary nonpolyposis colorectal neoplasms	GPathogenic
Select item 833349	NC_000002.12:g.(?_47403192)_(47408555_?)del	MSH2	Deletion	Hereditary nonpolyposis colorectal neoplasms	GPathogenic
Select item 584057	NC_000002.12:g.(?_47403182)_(47408565_?)del	MSH2	Deletion	Hereditary nonpolyposis colorectal neoplasms	GPathogenic
Select item 90492	NM_000251.1(MSH2):c.-4729_367-353del	LOC129933695, MSH2	Deletion	Lynch syndrome	GPathogenic

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