List of variants in gene ALOX12B reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001139.3(ALOX12B):c.1562A>G (p.Tyr521Cys)	rs199766569	0.00014
NM_001139.3(ALOX12B):c.1790C>A (p.Ala597Glu)	rs752509098	0.00005
NM_001139.3(ALOX12B):c.1642C>T (p.Arg548Trp)	rs397514532	0.00003
NM_001139.3(ALOX12B):c.1148C>T (p.Thr383Met)	rs760428119	0.00001
NM_001139.3(ALOX12B):c.340C>T (p.Arg114Trp)	rs397514526	0.00001
NM_001139.3(ALOX12B):c.1153del (p.Val385fs)	rs781409869

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