List of variants in gene ROGDI reported by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_024589.3(ROGDI):c.414G>A (p.Thr138=)	rs11553876	0.10521
NM_024589.3(ROGDI):c.393C>G (p.Asp131Glu)	rs143095485	0.01923
NM_024589.3(ROGDI):c.696C>T (p.Phe232=)	rs75818610	0.00686
NM_024589.3(ROGDI):c.646-5C>T	rs115660765	0.00647
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.567G>A (p.Leu189=)	rs143000899	0.00059
NM_024589.3(ROGDI):c.584A>G (p.Asn195Ser)	rs201116642	0.00006
NM_024589.3(ROGDI):c.555G>C (p.Pro185=)	rs771793763	0.00004
NM_024589.3(ROGDI):c.829G>A (p.Val277Met)	rs759234056	0.00002
NM_024589.3(ROGDI):c.117+10C>G	rs113858060
NM_024589.3(ROGDI):c.117+10C>T	rs113858060

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