List of variants in gene OSTM1 reported as benign by Illumina Laboratory Services, Illumina

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_014028.4(OSTM1):c.*331A>G	rs9320250	0.41485
NM_014028.4(OSTM1):c.*1883T>C	rs7662	0.33096
NM_014028.4(OSTM1):c.*2301A>G	rs9386700	0.32980
NM_014028.4(OSTM1):c.*1407A>G	rs12567	0.24864
NM_014028.4(OSTM1):c.*1038A>G	rs1064346	0.24805
NM_014028.4(OSTM1):c.*2283T>C	rs112283202	0.09569
NM_014028.4(OSTM1):c.*2344C>G	rs113263335	0.09290
NM_014028.4(OSTM1):c.*2329G>T	rs112792700	0.08905
NM_014028.4(OSTM1):c.*2755A>G	rs6921341	0.07269
NM_014028.4(OSTM1):c.*2547G>A	rs111332944	0.05196
NM_014028.4(OSTM1):c.*1161G>A	rs17069228	0.04528
NM_014028.4(OSTM1):c.*2887G>A	rs41287526	0.03905
NM_014028.4(OSTM1):c.*2053C>T	rs17069215	0.03750
NM_014028.4(OSTM1):c.*1352A>G	rs9372179	0.03746
NM_014028.4(OSTM1):c.*1334T>C	rs9374008	0.03745
NM_014028.4(OSTM1):c.*1574A>G	rs41287528	0.03604
NM_014028.4(OSTM1):c.*1367G>A	rs73504439	0.03564
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.*3329A>G	rs112424495	0.02226
NM_014028.4(OSTM1):c.*3319T>G	rs112919802	0.02222
NM_014028.4(OSTM1):c.221C>G (p.Pro74Arg)	rs141735624	0.01817
NM_014028.4(OSTM1):c.*212A>G	rs17069239	0.01518
NM_014028.4(OSTM1):c.*1427A>G	rs116796449	0.01274
NM_014028.4(OSTM1):c.*1082G>A	rs148730821	0.01114
NM_014028.4(OSTM1):c.*2138G>T	rs115370044	0.00824
NM_014028.4(OSTM1):c.*355A>G	rs61491262	0.00630
NM_014028.4(OSTM1):c.960C>G (p.Leu320=)	rs201793834	0.00001
NM_014028.4(OSTM1):c.*1441del	rs140320992

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