Variants in gene PMS2 with conflicting interpretations "uncertain significance" and "uncertain significance"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.2149G>A (p.Val717Met)	rs201671325	0.00072
NM_000535.7(PMS2):c.86G>C (p.Gly29Ala)	rs146176004	0.00059
NM_000535.7(PMS2):c.572A>G (p.Tyr191Cys)	rs375289386	0.00029
NM_000535.7(PMS2):c.53T>C (p.Ile18Thr)	rs201343342	0.00016
NM_000535.7(PMS2):c.2264T>C (p.Ile755Thr)	rs386833410	0.00002
NM_000535.7(PMS2):c.733C>A (p.Leu245Met)	rs201375580	0.00001
NM_000535.7(PMS2):c.695G>A (p.Gly232Glu)	rs201811667
NM_000535.7(PMS2):c.708G>T (p.Leu236Phe)	rs201395630
NM_000535.7(PMS2):c.858C>A (p.Asp286Glu)	rs201921616

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