List of variants in gene OSTM1 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_014028.4(OSTM1):c.402+267G>C	rs4946896	0.93343
NM_014028.4(OSTM1):c.615+226A>C	rs56237735	0.49865
NC_000006.12:g.108074962C>T	rs6568529	0.41270
NC_000006.12:g.108075062G>T	rs9320255	0.24686
NM_014028.4(OSTM1):c.615+113A>G	rs10484902	0.23686
NM_014028.4(OSTM1):c.950-166G>C	rs41287530	0.16465
NM_014028.4(OSTM1):c.783+27C>G	rs3757302	0.07231
NM_014028.4(OSTM1):c.518-255G>A	rs75259931	0.05030
NM_014028.4(OSTM1):c.207G>T (p.Gly69=)	rs80219951	0.03550
NM_014028.4(OSTM1):c.156G>C (p.Leu52Phe)	rs9480830	0.02937
NM_014028.4(OSTM1):c.615+21A>G	rs111735349	0.02233
NM_014028.4(OSTM1):c.221C>G (p.Pro74Arg)	rs141735624	0.01817
NM_014028.4(OSTM1):c.615+8A>G	rs144204437	0.00220
NM_014028.4(OSTM1):c.495A>G (p.Thr165=)	rs137974384	0.00110
NM_014028.4(OSTM1):c.177C>T (p.Ser59=)	rs377316819	0.00059
NM_014028.4(OSTM1):c.300G>T (p.Gly100=)	rs199570880	0.00014
NM_014028.4(OSTM1):c.960C>G (p.Leu320=)	rs201793834	0.00001
NM_014028.4(OSTM1):c.616-3del

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