ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.7575C>G (p.Pro2525=)

dbSNP: rs1569308187
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001093401 SCV001250359 likely benign not provided 2020-01-01 criteria provided, single submitter clinical testing
Invitae RCV003769031 SCV004683562 likely benign Duchenne muscular dystrophy 2023-08-28 criteria provided, single submitter clinical testing

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