ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.5715del (p.Lys1905fs)

dbSNP: rs2081171632
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Center, National Cancer Institute RCV001293812 SCV001481743 pathogenic Colorectal cancer no assertion criteria provided case-control

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