List of variants in gene combination OR10Z1, SPTA1 reported as uncertain significance for hematologic disorder

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003126.4(SPTA1):c.*68C>G	rs186892978	0.00406
NM_003126.4(SPTA1):c.*387T>C	rs549664412	0.00146
NM_003126.4(SPTA1):c.*341T>G	rs867313542	0.00008
NM_003126.4(SPTA1):c.*294A>G	rs886045378	0.00006
NM_003126.4(SPTA1):c.*39G>A	rs202171095	0.00006
NM_003126.4(SPTA1):c.*319C>T	rs561434223	0.00004
NM_003126.4(SPTA1):c.7198G>T (p.Gly2400Cys)	rs774112593	0.00003
NM_003126.4(SPTA1):c.*379G>A	rs976671141	0.00001
NM_003126.4(SPTA1):c.7228G>A (p.Val2410Ile)	rs750904139	0.00001
NM_003126.4(SPTA1):c.7237A>T (p.Thr2413Ser)	rs376198878	0.00001
NM_003126.4(SPTA1):c.*133C>T	rs868674912
NM_003126.4(SPTA1):c.*134T>G	rs866529035
NM_003126.4(SPTA1):c.*296G>T	rs886045377
NM_003126.4(SPTA1):c.*323T>C	rs867404163
NM_003126.4(SPTA1):c.*420T>A	rs1197068796
NM_003126.4(SPTA1):c.*509G>T	rs1649201828

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