ClinVar Miner

List of variants in gene MSH2 reported as likely benign for not provided

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Total variants: 40
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HGVS dbSNP
NM_000251.2(MSH2):c.-185C>A rs188036046
NM_000251.2(MSH2):c.-68-111C>T rs17224094
NM_000251.2(MSH2):c.-68-34T>C rs17217709
NM_000251.2(MSH2):c.1077-15G>T rs753277524
NM_000251.2(MSH2):c.108T>G (p.Leu36=) rs876659034
NM_000251.2(MSH2):c.1277-16T>C rs368653974
NM_000251.2(MSH2):c.132G>A (p.Thr44=) rs766856128
NM_000251.2(MSH2):c.1356A>G (p.Glu452=) rs63751212
NM_000251.2(MSH2):c.1387-14_1387-11delTGTT rs370436680
NM_000251.2(MSH2):c.1387-8G>T rs187525243
NM_000251.2(MSH2):c.1440A>G (p.Glu480=) rs138049198
NM_000251.2(MSH2):c.1488A>G (p.Leu496=) rs267607960
NM_000251.2(MSH2):c.1545C>T (p.Ser515=) rs1553366537
NM_000251.2(MSH2):c.159C>T (p.Ala53=) rs780178752
NM_000251.2(MSH2):c.1737A>G (p.Lys579=) rs61756467
NM_000251.2(MSH2):c.1787A>G (p.Asn596Ser) rs41295288
NM_000251.2(MSH2):c.1863A>T (p.Arg621=) rs786203119
NM_000251.2(MSH2):c.186G>A (p.Gly62=) rs750058876
NM_000251.2(MSH2):c.1963G>A (p.Val655Ile) rs549467183
NM_000251.2(MSH2):c.2006-15T>C rs1057524452
NM_000251.2(MSH2):c.2006-4G>A rs369853630
NM_000251.2(MSH2):c.2043A>G (p.Gln681=) rs730881763
NM_000251.2(MSH2):c.2094G>A (p.Glu698=) rs773555449
NM_000251.2(MSH2):c.211+8C>T rs267607916
NM_000251.2(MSH2):c.2154A>G (p.Gln718=) rs63750810
NM_000251.2(MSH2):c.2248T>C (p.Leu750=) rs527725593
NM_000251.2(MSH2):c.2500G>A (p.Ala834Thr) rs63750757
NM_000251.2(MSH2):c.2595C>T (p.Ile865=) rs547695133
NM_000251.2(MSH2):c.279_281delTCT (p.Leu94del) rs267607919
NM_000251.2(MSH2):c.2802G>A (p.Thr934=) rs150259097
NM_000251.2(MSH2):c.317G>A (p.Arg106Lys) rs41295286
NM_000251.2(MSH2):c.336C>A (p.Ser112=) rs34312619
NM_000251.2(MSH2):c.366+4A>C rs876659880
NM_000251.2(MSH2):c.499G>C (p.Asp167His) rs63750255
NM_000251.2(MSH2):c.4G>A (p.Ala2Thr) rs63750466
NM_000251.2(MSH2):c.55T>C (p.Phe19Leu) rs141711342
NM_000251.2(MSH2):c.606C>T (p.Pro202=) rs63750600
NM_000251.2(MSH2):c.762T>C (p.Asn254=) rs587779180
NM_000251.2(MSH2):c.819A>G (p.Val273=) rs146577635
NM_000251.2(MSH2):c.984C>T (p.Ala328=) rs4987189

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