List of variants in gene LOC130065472, SEC23B studied for anemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006363.5(SEC23B):c.-232C>G	rs4813333	0.83645
NM_006363.5(SEC23B):c.-186G>T	rs138178711	0.00524
NM_006363.5(SEC23B):c.-394A>C	rs561908920	0.00006
NM_006363.5(SEC23B):c.-283C>T	rs886056522
NM_006363.5(SEC23B):c.-301G>A	rs886056521

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