ClinVar Miner

Variants in gene ROGDI with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP
NM_024589.2(ROGDI):c.117+10C>G rs113858060
NM_024589.2(ROGDI):c.414G>A (p.Thr138=) rs11553876
NM_024589.2(ROGDI):c.522C>T (p.Ser174=) rs150687774
NM_024589.2(ROGDI):c.532-4G>A rs3747610
NM_024589.2(ROGDI):c.696-8G>T rs3747609
NM_024589.2(ROGDI):c.713G>A (p.Arg238His) rs138409264
NM_024589.2(ROGDI):c.823-10C>T rs199642172

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