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: 31

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HGVS	dbSNP	gnomAD frequency
NM_130837.3(OPA1):c.2332-19C>A	rs77355463	0.00155
NM_130837.3(OPA1):c.2872+15G>C	rs199763700	0.00126
NM_130837.3(OPA1):c.239A>G (p.Tyr80Cys)	rs151103940	0.00116
NM_130837.3(OPA1):c.2880A>G (p.Arg960=)	rs144898877	0.00107
NM_130837.3(OPA1):c.32+14C>T	rs201927764	0.00053
NM_130837.3(OPA1):c.2441-4dup	rs761286590	0.00017
NM_130837.3(OPA1):c.1377+10T>C	rs200114656	0.00007
NM_130837.3(OPA1):c.844-4G>A	rs377043223	0.00006
NM_130837.3(OPA1):c.2520+13A>G	rs371943802	0.00004
NM_130837.3(OPA1):c.2874T>C (p.Val958=)	rs773500478	0.00004
NM_130837.3(OPA1):c.611-9A>G	rs372157755	0.00003
NM_130837.3(OPA1):c.2812A>G (p.Ile938Val)	rs149866497	0.00002
NM_130837.3(OPA1):c.534A>G (p.Leu178=)	rs758901451	0.00002
NM_130837.3(OPA1):c.*6-13T>C	rs1243357575	0.00001
NM_130837.3(OPA1):c.-10C>T	rs775614028	0.00001
NM_130837.3(OPA1):c.1377+9A>G	rs759086025	0.00001
NM_130837.3(OPA1):c.1477+13A>G	rs1443336289	0.00001
NM_130837.3(OPA1):c.1871-19A>C	rs1057522968	0.00001
NM_130837.3(OPA1):c.1935+17C>T	rs769085336	0.00001
NM_130837.3(OPA1):c.2012+7A>G	rs767488490	0.00001
NM_130837.3(OPA1):c.205C>G (p.Pro69Ala)	rs750775588	0.00001
NM_130837.3(OPA1):c.2229G>A (p.Pro743=)	rs768448865	0.00001
NM_130837.3(OPA1):c.2250C>T (p.Asp750=)	rs769658263	0.00001
NM_130837.3(OPA1):c.581T>C (p.Ile194Thr)	rs1294430125	0.00001
NM_130837.3(OPA1):c.-11C>G	rs568049951
NM_130837.3(OPA1):c.113_130del (p.Arg38_Ser43del)	rs863224140
NM_130837.3(OPA1):c.1936-21_1936-18del	rs765277368
NM_130837.3(OPA1):c.2064T>C (p.Ile688=)
NM_130837.3(OPA1):c.2441-13T>A	rs773828534
NM_130837.3(OPA1):c.2973G>C (p.Ala991=)	rs117475774
NM_130837.3(OPA1):c.679-7G>T	rs373326620

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