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Q50894957-2EDA9F29-734D-4C66-8483-AB86AF1B7F47
Q50894957-2EDA9F29-734D-4C66-8483-AB86AF1B7F47
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Statement
http://www.wikidata.org/entity/statement/Q50894957-2EDA9F29-734D-4C66-8483-AB86AF1B7F47
The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families.
P2860
Q50894957-2EDA9F29-734D-4C66-8483-AB86AF1B7F47
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50894957-2EDA9F29-734D-4C66-8483-AB86AF1B7F47
rank
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wasDerivedFrom
821ef13a786773b7e410ae4f6fb5f117eb9dd78b
P2860
The HNPCC associated MSH2*1906G-->C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population.