List of variants in gene combination SARM1, SLC46A1 reported as likely benign for anemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_080669.6(SLC46A1):c.*4316C>G	rs117397871	0.01065
NM_080669.6(SLC46A1):c.*2123G>C	rs7225850	0.00854
NM_080669.6(SLC46A1):c.*3120A>G	rs147971222	0.00348
NM_080669.6(SLC46A1):c.*1648G>A	rs114008979	0.00295
NM_080669.6(SLC46A1):c.*2852C>T	rs569526091	0.00243
NM_080669.6(SLC46A1):c.*1332G>A	rs146041886	0.00101
NM_080669.6(SLC46A1):c.*1392C>A	rs141940033	0.00011
NM_080669.6(SLC46A1):c.*60G>T	rs41297121	0.00006
NM_080669.6(SLC46A1):c.1214C>T (p.Thr405Met)	rs541069777	0.00002
NM_080669.6(SLC46A1):c.*4035G>A	rs569679076

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