ClinVar Miner

List of variants reported as likely pathogenic for adenocarcinoma by Mendelics

Included ClinVar conditions (108):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001904.4(CTNNB1):c.1530dup (p.Val511fs) rs1575330336
NM_004360.5(CDH1):c.1009-1G>C rs1597894632
NM_004360.5(CDH1):c.2439+1G>T rs1567516230
NM_024529.5(CDC73):c.1450C>T (p.Arg484Cys) rs1225502334

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