ClinVar Miner

List of variants in gene MSH2 reported as likely pathogenic for endometrial disorder

Included ClinVar conditions (17):

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_000251.3(MSH2):c.1045C>A (p.Pro349Thr)	rs267607939

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