ClinVar Miner

Submissions for variant NM_000324.3(RHAG):c.154_157delinsGA (p.Pro52fs)

dbSNP: rs387906519
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013932 SCV000034179 pathogenic Rh-null, regulator type 1996-02-01 no assertion criteria provided literature only

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