ClinVar Miner

List of variants reported as pathogenic for Rh-null, regulator type

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Total variants: 8
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HGVS dbSNP
NM_000324.2(RHAG):c.1067+1G>A rs1562012617
NM_000324.2(RHAG):c.1086del (p.Ala363fs) rs1562011389
NM_000324.2(RHAG):c.1139G>T (p.Gly380Val) rs121918589
NM_000324.2(RHAG):c.154_157delinsGA (p.Pro52fs) rs387906519
NM_000324.2(RHAG):c.157+1G>A rs375508949
NM_000324.2(RHAG):c.836G>A (p.Gly279Glu) rs121918587
NM_000324.2(RHAG):c.946-1G>A rs1562012697
NM_000324.2(RHAG):c.[808G>A;838G>A]

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