ClinVar Miner

List of variants reported as likely pathogenic for Lynch syndrome by Human Genome Sequencing Center Clinical Lab,Baylor College of Medicine

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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NM_000179.2(MSH6):c.3226C>T (p.Arg1076Cys) rs63750617
NM_000249.3(MLH1):c.677G>T (p.Arg226Leu) rs63751711
NM_000535.7(PMS2):c.614A>C (p.Gln205Pro) rs587779342
NM_000535.7(PMS2):c.873del (p.Phe291fs) rs1261282733

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