List of variants in gene OPA1 reported as likely benign for not specified

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: 33

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HGVS	dbSNP
NM_015560.2(OPA1):c.*6-13T>C	rs1243357575
NM_015560.2(OPA1):c.-10C>T	rs775614028
NM_015560.2(OPA1):c.-11C>G	rs568049951
NM_015560.2(OPA1):c.1212+10T>C	rs200114656
NM_015560.2(OPA1):c.1212+9A>G	rs759086025
NM_015560.2(OPA1):c.1705+17A>G	rs749368763
NM_015560.2(OPA1):c.1706-19A>C	rs1057522968
NM_015560.2(OPA1):c.1771-21_1771-18del	rs765277368
NM_015560.2(OPA1):c.182A>G (p.Gln61Arg)	rs558532319
NM_015560.2(OPA1):c.1847+7A>G	rs767488490
NM_015560.2(OPA1):c.1863A>G (p.Gln621=)	rs773826671
NM_015560.2(OPA1):c.1923G>A (p.Ala641=)	rs138114609
NM_015560.2(OPA1):c.205C>G (p.Pro69Ala)	rs750775588
NM_015560.2(OPA1):c.2064G>A (p.Pro688=)	rs768448865
NM_015560.2(OPA1):c.2167-19C>A	rs77355463
NM_015560.2(OPA1):c.2276-13T>A	rs773828534
NM_015560.2(OPA1):c.2276-4dup	rs761286590
NM_015560.2(OPA1):c.2355+13A>G	rs371943802
NM_015560.2(OPA1):c.239A>G (p.Tyr80Cys)	rs151103940
NM_015560.2(OPA1):c.2427T>C (p.Leu809=)	rs145999595
NM_015560.2(OPA1):c.2647A>G (p.Ile883Val)	rs149866497
NM_015560.2(OPA1):c.2707+15G>C	rs199763700
NM_015560.2(OPA1):c.2715A>G (p.Arg905=)	rs144898877
NM_015560.2(OPA1):c.2808G>C (p.Ala936=)	rs117475774
NM_015560.2(OPA1):c.32+14C>T	rs201927764
NM_015560.2(OPA1):c.534A>G (p.Leu178=)	rs758901451
NM_015560.2(OPA1):c.565G>A (p.Glu189Lys)	rs569675223
NM_015560.2(OPA1):c.625-5527G>T	rs373326620
NM_015560.2(OPA1):c.679-4G>A	rs377043223
NM_015560.2(OPA1):c.70A>G (p.Ile24Val)	rs201520438
NM_015560.2(OPA1):c.756C>T (p.Asp252=)	rs147242797
NM_015560.2(OPA1):c.784-11A>C	rs376681712
NM_015560.2(OPA1):c.784-12_784-11insTA	rs544490050

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