List of variants in gene MSH2 reported as uncertain significance by True Health Diagnostics

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.1461C>G (p.Asp487Glu)	rs35107951	0.00011
NM_000251.3(MSH2):c.1045C>G (p.Pro349Ala)	rs267607939	0.00007
NM_000251.3(MSH2):c.382C>G (p.Leu128Val)	rs145649774	0.00006
NM_000251.3(MSH2):c.1601G>A (p.Arg534His)	rs587778523	0.00004
NM_000251.3(MSH2):c.2528G>A (p.Cys843Tyr)	rs747700106	0.00003
NM_000251.3(MSH2):c.894G>C (p.Gln298His)	rs587781397	0.00002
NM_000251.3(MSH2):c.2483T>G (p.Ile828Ser)	rs753067992
NM_000251.3(MSH2):c.79C>A (p.Pro27Thr)	rs878853826

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