ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2698G>A (p.Gly900Arg)

dbSNP: rs1553245908
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000516459 SCV000612442 likely pathogenic not provided 2017-01-31 criteria provided, single submitter clinical testing

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