ClinVar Miner

List of variants in gene combination LOC129933695, MSH2 reported as not provided for Lynch syndrome 1

Included ClinVar conditions (5):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_000251.1(MSH2):c.-823_1076+5984del

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