ClinVar Miner

List of variants reported as likely pathogenic by True Health Diagnostics

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Minimum conflict level:
ClinVar version:
Total variants: 5
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NM_000059.4(BRCA2):c.9004G>A (p.Glu3002Lys) rs80359152
NM_000179.2(MSH6):c.1513dup (p.Tyr505fs) rs1553412912
NM_007194.4(CHEK2):c.190G>A (p.Glu64Lys) rs141568342
NM_007194.4(CHEK2):c.499G>A (p.Gly167Arg) rs72552322
NM_007194.4(CHEK2):c.917G>C (p.Gly306Ala) rs587780192

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