ClinVar Miner

Submissions for variant NM_000324.3(RHAG):c.3G>T (p.Met1Ile)

gnomAD frequency: 0.00001  dbSNP: rs121918588
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000013938 SCV000034185 pathogenic Rh mod blood group phenotype 1998-09-01 no assertion criteria provided literature only

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