List of variants in gene OTC reported as benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001407092.1(OTC):c.-79-582C>T	rs5963412	0.69728
NM_001407092.1(OTC):c.-79-567G>A	rs5963413	0.69374
NM_000531.6(OTC):c.1005+941T>C	rs5963419	0.51422
NM_000531.6(OTC):c.540+134G>A	rs2272721	0.50169
NM_000531.6(OTC):c.541-63G>A	rs2235125	0.46334
NM_000531.6(OTC):c.541-172_541-170dup	rs3047852	0.46083
NM_000531.6(OTC):c.137A>G (p.Lys46Arg)	rs1800321	0.26575
NM_000531.6(OTC):c.541-305A>G	rs6609709	0.22631
NM_000531.6(OTC):c.1006-70C>T	rs12557315	0.18755
NM_000531.6(OTC):c.664-220G>A	rs1554993	0.13567
NM_000531.6(OTC):c.540+455A>G	rs12855364	0.12268
NM_000531.6(OTC):c.718-14T>C	rs55722856	0.05854
NM_000531.6(OTC):c.809A>G (p.Gln270Arg)	rs1800328	0.02868
NM_000531.6(OTC):c.1005+1133A>G	rs56125451	0.02726
NM_000531.6(OTC):c.867+35T>G	rs62622415	0.02489
NM_000531.6(OTC):c.78-233G>C	rs148036282	0.02409
NM_000531.6(OTC):c.217-200G>A	rs7064359	0.02350
NM_000531.6(OTC):c.867+905T>C	rs144339942	0.02205
NM_000531.6(OTC):c.540+203C>A	rs7057582	0.01817
NM_000531.6(OTC):c.540+489A>G	rs148514349	0.01609
NM_000531.6(OTC):c.299-18C>T	rs5917586	0.00006
NC_000023.11:g.38352178TTCT[1]	rs57752938
NM_000531.6(OTC):c.1005+132dup	rs3215429
NM_000531.6(OTC):c.216+280ATTT[7]	rs200633699
NM_000531.6(OTC):c.217-265del	rs11313102
NM_000531.6(OTC):c.217-266_217-265del	rs11313102
NM_000531.6(OTC):c.299-34dup	rs398122026
NM_000531.6(OTC):c.664-287C>T	rs141787318
NM_000531.6(OTC):c.78-103dup	rs755821521
NM_000531.6(OTC):c.868-182dup	rs368534980

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