List of variants in gene CYBA reported as 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000101.4(CYBA):c.521T>C (p.Val174Ala)	rs1049254	0.68722
NM_000101.4(CYBA):c.214T>C (p.Tyr72His)	rs4673	0.64973
NM_000101.4(CYBA):c.203+8T>C	rs4782393	0.44118
NM_000101.4(CYBA):c.268C>T (p.Arg90Trp)	rs179363892	0.00006
NM_000101.4(CYBA):c.155T>C (p.Leu52Pro)	rs179363890	0.00003
NM_000101.4(CYBA):c.371C>T (p.Ala124Val)	rs179363894	0.00003
NM_000101.4(CYBA):c.193A>G (p.Met65Val)	rs1567609300	0.00001
NM_000101.4(CYBA):c.158A>T (p.Glu53Val)	rs179363893
NM_000101.4(CYBA):c.354C>A (p.Ser118Arg)	rs104894514
NM_000101.4(CYBA):c.467C>A (p.Pro156Gln)	rs104894515
NM_000101.4(CYBA):c.74G>T (p.Gly25Val)	rs179363891

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