List of variants in gene MSH2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.435T>G (p.Ile145Met)	rs63750124	0.00031
NM_000251.3(MSH2):c.1787A>G (p.Asn596Ser)	rs41295288	0.00022
NM_000251.3(MSH2):c.1748A>G (p.Asn583Ser)	rs201118107	0.00014
NM_000251.3(MSH2):c.128A>G (p.Tyr43Cys)	rs17217723	0.00011
NM_000251.3(MSH2):c.508C>G (p.Gln170Glu)	rs63750843	0.00011
NM_000251.3(MSH2):c.-181G>A	rs786201698	0.00010
NM_000251.3(MSH2):c.97A>C (p.Thr33Pro)	rs63751107	0.00009
NM_000251.3(MSH2):c.1217G>A (p.Arg406Gln)	rs146567853	0.00008
NM_000251.3(MSH2):c.1045C>G (p.Pro349Ala)	rs267607939	0.00007
NM_000251.3(MSH2):c.1238A>C (p.Gln413Pro)	rs587779962	0.00004
NM_000251.3(MSH2):c.2516A>G (p.His839Arg)	rs63750027	0.00004
NM_000251.3(MSH2):c.991A>G (p.Asn331Asp)	rs267607938	0.00003
NM_000251.3(MSH2):c.2009C>T (p.Pro670Leu)	rs41294982	0.00002
NM_000251.3(MSH2):c.1254A>G (p.Ile418Met)	rs751431238	0.00001
NM_000251.3(MSH2):c.1480T>C (p.Ser494Pro)	rs55653533	0.00001
NM_000251.3(MSH2):c.1802A>G (p.Gln601Arg)	rs779447213	0.00001
NM_000251.3(MSH2):c.1825G>T (p.Ala609Ser)	rs150980616	0.00001
NM_000251.3(MSH2):c.1927G>A (p.Glu643Lys)	rs374840361	0.00001
NM_000251.3(MSH2):c.220A>C (p.Asn74His)	rs150548839	0.00001
NM_000251.3(MSH2):c.376G>A (p.Gly126Ser)	rs767371843	0.00001
NM_000251.3(MSH2):c.566C>G (p.Ala189Gly)	rs141021599	0.00001
NM_000251.3(MSH2):c.610G>A (p.Gly204Arg)	rs63750574	0.00001
NM_000251.3(MSH2):c.992A>G (p.Asn331Ser)	rs779673318	0.00001
NM_000251.3(MSH2):c.1354G>A (p.Glu452Lys)	rs267607954
NM_000251.3(MSH2):c.1454T>C (p.Met485Thr)	rs1553365763
NM_000251.3(MSH2):c.166G>A (p.Glu56Lys)	rs587779102
NM_000251.3(MSH2):c.1688A>G (p.Tyr563Cys)	rs63751054
NM_000251.3(MSH2):c.1892G>A (p.Arg631Lys)	rs1361816581
NM_000251.3(MSH2):c.1A>C (p.Met1Leu)	rs267607911
NM_000251.3(MSH2):c.2065G>A (p.Ala689Thr)	rs914610419
NM_000251.3(MSH2):c.2260A>G (p.Thr754Ala)	rs757268664
NM_000251.3(MSH2):c.2260A>T (p.Thr754Ser)	rs757268664
NM_000251.3(MSH2):c.383T>G (p.Leu128Arg)	rs730881768
NM_000251.3(MSH2):c.464T>C (p.Val155Ala)	rs876658188
NM_000251.3(MSH2):c.73G>T (p.Gly25Cys)	rs746259256
NM_000251.3(MSH2):c.943G>T (p.Gly315Cys)	rs2104242161

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