List of variants in gene ROGDI reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_024589.3(ROGDI):c.713G>A (p.Arg238His)	rs138409264	0.00548
NM_024589.3(ROGDI):c.522C>T (p.Ser174=)	rs150687774	0.00190
NM_024589.3(ROGDI):c.810G>A (p.Gln270=)	rs137912684	0.00139
NM_024589.3(ROGDI):c.567G>A (p.Leu189=)	rs143000899	0.00059
NM_024589.3(ROGDI):c.489C>T (p.Pro163=)	rs113245789	0.00056
NM_024589.3(ROGDI):c.378G>C (p.Leu126=)	rs145588848	0.00026
NM_024589.3(ROGDI):c.532-4G>A	rs3747610	0.00017
NM_024589.3(ROGDI):c.669G>A (p.Ala223=)	rs143402543	0.00006
NM_024589.3(ROGDI):c.187C>T (p.Leu63=)	rs372790777	0.00003
NM_024589.3(ROGDI):c.507C>T (p.Pro169=)	rs767771299	0.00001
NM_024589.3(ROGDI):c.514G>A (p.Ala172Thr)	rs201213891	0.00001
NM_024589.3(ROGDI):c.255+22C>T
NM_024589.3(ROGDI):c.66G>A (p.Leu22=)	rs1452732971
NM_024589.3(ROGDI):c.705C>A (p.Gly235=)	rs2082671081

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