List of variants in gene PMS2 reported as likely pathogenic for uterine disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.2249G>A (p.Gly750Asp)	rs587779337	0.00001
NM_000535.7(PMS2):c.134A>C (p.Asn45Thr)	rs1554306353
NM_000535.7(PMS2):c.137G>A (p.Ser46Asn)	rs121434629

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