ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.3114-20A>G

gnomAD frequency: 0.00001  dbSNP: rs770731003
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002173256 SCV002350327 likely benign Familial cancer of breast 2021-06-16 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002173256 SCV004020161 benign Familial cancer of breast 2023-03-08 criteria provided, single submitter clinical testing This variant is considered benign. Homozygosity for this variant has been confirmed in one or more individuals lacking clinical features consistent with gene-specific recessive disease, indicating that this variant is unlikely to be pathogenic.

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