ClinVar Miner

Submissions for variant NM_005235.3(ERBB4):c.3814G>A (p.Gly1272Arg)

dbSNP: rs371332509
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
UM ALS/MND Lab, University Of Malta RCV001260557 SCV001426208 likely pathogenic Amyotrophic lateral sclerosis 2020-07-31 criteria provided, single submitter case-control

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